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dbVar

Database of genomic structural variation

nsv5633153

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: 233 SVs from 23 studies. See in: genome view

Submitted genomic26,590,410-26,590,410

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5633153	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	26,590,410	26,590,410
nsv5633153	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	26,447,926	26,447,926

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17147006	insertion	HG00512	Sequencing	Sequence alignment	6,637

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17147006	Submitted genomic		NC_000008.11:g.265 90410_26590411ins6 1	GRCh38 (hg38)		NC_000008.11	Chr8	26,590,410	26,590,410
nssv17147006	Remapped	Perfect	NC_000008.10:g.264 47926_26447927ins6 1	GRCh37.p13	First Pass	NC_000008.10	Chr8	26,447,926	26,447,926

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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