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dbVar

Database of genomic structural variation

nsv5660665

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: 297 SVs from 31 studies. See in: genome view

Submitted genomic113,727,623-113,727,623

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5660665	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000013.11	Chr13	113,727,623	113,727,623
nsv5660665	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000013.10	Chr13	114,430,596	114,430,596

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17083253	insertion	HG02011	Sequencing	Sequence alignment	2,906

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17083253	Submitted genomic		NC_000013.11:g.113 727623_113727624in s55	GRCh38 (hg38)		NC_000013.11	Chr13	113,727,623	113,727,623
nssv17083253	Remapped	Perfect	NC_000013.10:g.114 430596_114430597in s55	GRCh37.p13	First Pass	NC_000013.10	Chr13	114,430,596	114,430,596

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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