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dbVar

Database of genomic structural variation

nsv5647862

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: 127 SVs from 27 studies. See in: genome view

Submitted genomic14,554,505-14,554,505

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5647862	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	14,554,505	14,554,505
nsv5647862	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	14,665,317	14,665,317

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17103182	insertion	SAMN00249812	Sequencing	Sequence alignment	1,255

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17103182	Submitted genomic		NC_000019.10:g.145 54505_14554506ins1 274	GRCh38 (hg38)		NC_000019.10	Chr19	14,554,505	14,554,505
nssv17103182	Remapped	Perfect	NC_000019.9:g.1466 5317_14665318ins12 74	GRCh37.p13	First Pass	NC_000019.9	Chr19	14,665,317	14,665,317

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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