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dbVar

Database of genomic structural variation

nsv6112635

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

Submitted genomic41,294,883-41,294,883

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6112635	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	41,294,883	41,294,883
nsv6112635	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	41,690,887	41,690,887

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17642246	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17642246	Submitted genomic		NC_000022.11:g.412 94883_41294884ins2 87	GRCh38 (hg38)		NC_000022.11	Chr22	41,294,883	41,294,883
nssv17642246	Remapped	Perfect	NC_000022.10:g.416 90887_41690888ins2 87	GRCh37.p13	First Pass	NC_000022.10	Chr22	41,690,887	41,690,887

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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