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dbVar

Database of genomic structural variation

nsv2820931

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: 429 SVs from 25 studies. See in: genome view

Submitted genomic85,911,199-85,911,199

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv2820931	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	85,911,199	85,911,199
nsv2820931	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	85,166,204	85,166,204

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv13711073	insertion	Sequencing	Genotyping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv13711073	Submitted genomic		NC_000023.11:g.859 11199_85911200ins3 03	GRCh38 (hg38)		NC_000023.11	ChrX	85,911,199	85,911,199
nssv13711073	Remapped	Perfect	NC_000023.10:g.851 66204_85166205ins3 03	GRCh37.p13	First Pass	NC_000023.10	ChrX	85,166,204	85,166,204

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)
nssv13711073	0.828	53	64

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