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dbVar

Database of genomic structural variation

nsv6112626

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: 536 SVs from 31 studies. See in: genome view

Submitted genomic50,608,687-50,608,687

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6112626	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	50,608,687	50,608,687
nsv6112626	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	51,047,115	51,047,115

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17646002	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17646002	Submitted genomic		NC_000022.11:g.506 08687_50608688ins6 3	GRCh38 (hg38)		NC_000022.11	Chr22	50,608,687	50,608,687
nssv17646002	Remapped	Perfect	NC_000022.10:g.510 47115_51047116ins6 3	GRCh37.p13	First Pass	NC_000022.10	Chr22	51,047,115	51,047,115

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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