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dbVar

Database of genomic structural variation

nsv6111913

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: 334 SVs from 40 studies. See in: genome view

Submitted genomic404,810-404,810

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6111913	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	404,810	404,810
nsv6111913	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	404,810	404,810

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17630338	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17630338	Submitted genomic		NC_000019.10:g.404 810_404811ins290	GRCh38 (hg38)		NC_000019.10	Chr19	404,810	404,810
nssv17630338	Remapped	Perfect	NC_000019.9:g.4048 10_404811ins290	GRCh37.p13	First Pass	NC_000019.9	Chr19	404,810	404,810

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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