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dbVar

Database of genomic structural variation

nsv6029807

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:274

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: 141 SVs from 37 studies. See in: genome view

Submitted genomic100,873,202-100,873,475

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6029807	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	100,873,202	100,873,475
nsv6029807	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	101,339,539	101,339,812

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17601021	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17601021	Submitted genomic		NC_000014.9:g.1008 73202_100873475dup	GRCh38 (hg38)		NC_000014.9	Chr14	100,873,202	100,873,475
nssv17601021	Remapped	Perfect	NC_000014.8:g.1013 39539_101339812dup	GRCh37.p13	First Pass	NC_000014.8	Chr14	101,339,539	101,339,812

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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