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dbVar

Database of genomic structural variation

nsv5630936

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: 338 SVs from 48 studies. See in: genome view

Submitted genomic170,398,770-170,398,770

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5630936	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	170,398,770	170,398,770
nsv5630936	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	170,707,858	170,707,858

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17157881	insertion	SAMN00007703	Sequencing	Sequence alignment	1,054

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17157881	Submitted genomic		NC_000006.12:g.170 398770_170398771in s1670	GRCh38 (hg38)		NC_000006.12	Chr6	170,398,770	170,398,770
nssv17157881	Remapped	Perfect	NC_000006.11:g.170 707858_170707859in s1670	GRCh37.p13	First Pass	NC_000006.11	Chr6	170,707,858	170,707,858

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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