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dbVar

Database of genomic structural variation

nsv5667669

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: 258 SVs from 44 studies. See in: genome view

Submitted genomic62,321,452-62,321,452

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5667669	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	62,321,452	62,321,452
nsv5667669	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	60,896,508	60,896,508

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17117417	insertion	HG03732	Sequencing	Sequence alignment	1,582

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17117417	Submitted genomic		NC_000020.11:g.623 21452_62321453ins1 89	GRCh38 (hg38)		NC_000020.11	Chr20	62,321,452	62,321,452
nssv17117417	Remapped	Perfect	NC_000020.10:g.608 96508_60896509ins1 89	GRCh37.p13	First Pass	NC_000020.10	Chr20	60,896,508	60,896,508

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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