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dbVar

Database of genomic structural variation

nsv5628915

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Ebert et al. 2021

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: 100 SVs from 19 studies. See in: genome view

Submitted genomic143,814,595-143,814,595

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5628915	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	143,814,595	143,814,595
nsv5628915	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	144,135,732	144,135,732

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17143550	insertion	HG03683	Sequencing	Sequence alignment	2,232

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17143550	Submitted genomic		NC_000006.12:g.143 814595_143814596in s66	GRCh38 (hg38)		NC_000006.12	Chr6	143,814,595	143,814,595
nssv17143550	Remapped	Perfect	NC_000006.11:g.144 135732_144135733in s66	GRCh37.p13	First Pass	NC_000006.11	Chr6	144,135,732	144,135,732

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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