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dbVar

Database of genomic structural variation

nsv6110259

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: 96 SVs from 23 studies. See in: genome view

Submitted genomic46,027,693-46,027,693

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6110259	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	46,027,693	46,027,693
nsv6110259	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	46,530,951	46,530,951

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17625774	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17625774	Submitted genomic		NC_000019.10:g.460 27693_46027694ins1 03	GRCh38 (hg38)		NC_000019.10	Chr19	46,027,693	46,027,693
nssv17625774	Remapped	Perfect	NC_000019.9:g.4653 0951_46530952ins10 3	GRCh37.p13	First Pass	NC_000019.9	Chr19	46,530,951	46,530,951

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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