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dbVar

Database of genomic structural variation

nsv2820949

Organism: Homo sapiens

Study:nstd137 (Huddleston et al. 2016)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38 (hg38)

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

Publication(s):Huddleston et al. 2016

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: 431 SVs from 36 studies. See in: genome view

Submitted genomic90,236,966-90,236,966

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv2820949	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	90,236,966	90,236,966
nsv2820949	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	89,491,965	89,491,965

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv13700410	insertion	Sequencing	Genotyping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv13700410	Submitted genomic		NC_000023.11:g.902 36966_90236967ins1 739	GRCh38 (hg38)		NC_000023.11	ChrX	90,236,966	90,236,966
nssv13700410	Remapped	Perfect	NC_000023.10:g.894 91965_89491966ins1 739	GRCh37.p13	First Pass	NC_000023.10	ChrX	89,491,965	89,491,965

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv13700410	0.016	1	64

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