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dbVar

Database of genomic structural variation

nsv6017873

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:246

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: 103 SVs from 25 studies. See in: genome view

Submitted genomic54,759,207-54,759,452

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6017873	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	54,759,207	54,759,452
nsv6017873	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	54,826,900	54,827,145

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17567997	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17567997	Submitted genomic		NC_000007.14:g.547 59207_54759452del	GRCh38 (hg38)		NC_000007.14	Chr7	54,759,207	54,759,452
nssv17567997	Remapped	Perfect	NC_000007.13:g.548 26900_54827145del	GRCh37.p13	First Pass	NC_000007.13	Chr7	54,826,900	54,827,145

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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