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dbVar

Database of genomic structural variation

nsv6112615

Organism: Homo sapiens

Study:nstd212 (Wu 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):Wu 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: 401 SVs from 43 studies. See in: genome view

Submitted genomic46,294,027-46,294,027

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6112615	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000021.9	Chr21	46,294,027	46,294,027
nsv6112615	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000021.8	Chr21	47,713,941	47,713,941

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17639190	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17639190	Submitted genomic		NC_000021.9:g.4629 4027_46294028ins74	GRCh38 (hg38)		NC_000021.9	Chr21	46,294,027	46,294,027
nssv17639190	Remapped	Perfect	NC_000021.8:g.4771 3941_47713942ins74	GRCh37.p13	First Pass	NC_000021.8	Chr21	47,713,941	47,713,941

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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