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dbVar

Database of genomic structural variation

nsv6112659

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: 296 SVs from 42 studies. See in: genome view

Submitted genomic404,996-404,996

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6112659	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	404,996	404,996
nsv6112659	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	404,996	404,996

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17618063	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17618063	Submitted genomic		NC_000019.10:g.404 996_404997ins194	GRCh38 (hg38)		NC_000019.10	Chr19	404,996	404,996
nssv17618063	Remapped	Perfect	NC_000019.9:g.4049 96_404997ins194	GRCh37.p13	First Pass	NC_000019.9	Chr19	404,996	404,996

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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