Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv4909841

Organism: Homo sapiens

Study:nstd200 (Abel et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1,320

Publication(s):Abel et al. 2020

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 145 SVs from 21 studies. See in: genome view

Submitted genomic178,471,336-178,472,714

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4909841	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	178,471,366 (-30, +66)	178,472,685 (-40, +29)
nsv4909841	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	179,336,093 (-30, +66)	179,337,412 (-40, +29)

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16439978	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16439978	Submitted genomic		NC_000002.12:g.(17 8471336_178471432) _(178472645_178472 714)del	GRCh38 (hg38)		NC_000002.12	Chr2	178,471,366 (-30, +66)	178,472,685 (-40, +29)
nssv16439978	Remapped	Perfect	NC_000002.11:g.(17 9336063_179336159) _(179337372_179337 441)del	GRCh37.p13	First Pass	NC_000002.11	Chr2	179,336,093 (-30, +66)	179,337,412 (-40, +29)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16439978	<0.001	2	29246

You are here: NCBI