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dbVar

Database of genomic structural variation

nsv2820886

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: 379 SVs from 26 studies. See in: genome view

Submitted genomic66,037,122-66,037,122

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv2820886	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	66,037,122	66,037,122
nsv2820886	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	65,256,964	65,256,964

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv13697619	insertion	Sequencing	Genotyping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv13697619	Submitted genomic		NC_000023.11:g.660 37122_66037123ins5 91	GRCh38 (hg38)		NC_000023.11	ChrX	66,037,122	66,037,122
nssv13697619	Remapped	Perfect	NC_000023.10:g.652 56964_65256965ins5 91	GRCh37.p13	First Pass	NC_000023.10	ChrX	65,256,964	65,256,964

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)
nssv13697619	1	58	58

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