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dbVar

Database of genomic structural variation

nsv5617721

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: 159 SVs from 34 studies. See in: genome view

Submitted genomic86,634,068-86,634,068

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5617721	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	86,634,068	86,634,068
nsv5617721	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	87,099,751	87,099,751

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17066544	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
nssv17066544	Submitted genomic		NC_000001.11:g.866 34068_86634069ins1 345	GRCh38 (hg38)		NC_000001.11	Chr1	86,634,068	86,634,068
nssv17066544	Remapped	Perfect	NC_000001.10:g.870 99751_87099752ins1 345	GRCh37.p13	First Pass	NC_000001.10	Chr1	87,099,751	87,099,751

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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