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dbVar

Database of genomic structural variation

nsv5620627

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: 146 SVs from 28 studies. See in: genome view

Submitted genomic60,004,924-60,004,924

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5620627	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	60,004,924	60,004,924
nsv5620627	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	60,470,596	60,470,596

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17065887	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
nssv17065887	Submitted genomic		NC_000001.11:g.600 04924_60004925ins3 35	GRCh38 (hg38)		NC_000001.11	Chr1	60,004,924	60,004,924
nssv17065887	Remapped	Perfect	NC_000001.10:g.604 70596_60470597ins3 35	GRCh37.p13	First Pass	NC_000001.10	Chr1	60,470,596	60,470,596

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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