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dbVar

Database of genomic structural variation

nsv6040741

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:84

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: 139 SVs from 27 studies. See in: genome view

Submitted genomic17,299,276-17,299,359

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6040741	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	17,299,276	17,299,359
nsv6040741	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	17,410,085	17,410,168

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17628538	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17628538	Submitted genomic		NC_000019.10:g.172 99276_17299359del	GRCh38 (hg38)		NC_000019.10	Chr19	17,299,276	17,299,359
nssv17628538	Remapped	Perfect	NC_000019.9:g.1741 0085_17410168del	GRCh37.p13	First Pass	NC_000019.9	Chr19	17,410,085	17,410,168

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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