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dbVar

Database of genomic structural variation

nsv5645879

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

Submitted genomic74,229,477-74,229,477

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5645879	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	74,229,477	74,229,477
nsv5645879	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	73,940,522	73,940,522

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17075867	insertion	HG02587	Sequencing	Sequence alignment	2,330

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17075867	Submitted genomic		NC_000011.10:g.742 29477_74229478ins3 32	GRCh38 (hg38)		NC_000011.10	Chr11	74,229,477	74,229,477
nssv17075867	Remapped	Perfect	NC_000011.9:g.7394 0522_73940523ins33 2	GRCh37.p13	First Pass	NC_000011.9	Chr11	73,940,522	73,940,522

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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