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dbVar

Database of genomic structural variation

nsv6021873

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:270,845

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: 1563 SVs from 93 studies. See in: genome view

Submitted genomic40,936,251-41,207,095

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6021873	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	40,936,251	41,207,095
nsv6021873	Remapped	Good	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	41,405,456	41,676,298

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17600920	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17600920	Submitted genomic		NC_000014.9:g.4093 6251_41207095del	GRCh38 (hg38)		NC_000014.9	Chr14	40,936,251	41,207,095
nssv17600920	Remapped	Good	NC_000014.8:g.4140 5456_41676298del	GRCh37.p13	First Pass	NC_000014.8	Chr14	41,405,456	41,676,298

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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