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dbVar

Database of genomic structural variation

nsv4730449

Organism: Homo sapiens

Study:nstd199 (Quan et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:70

Publication(s):Quan 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: 80 SVs from 20 studies. See in: genome view

Remapped(Score: Perfect):25,058,689-25,058,758

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4730449	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000010.11	Chr10	25,058,689	25,058,758
nsv4730449	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000010.10	Chr10	25,347,618	25,347,687

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16267273	deletion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16267273	Remapped	Perfect	NC_000010.11:g.250 58689_25058758del	GRCh38.p12	First Pass	NC_000010.11	Chr10	25,058,689	25,058,758
nssv16267273	Submitted genomic		NC_000010.10:g.253 47618_25347687del	GRCh37 (hg19)		NC_000010.10	Chr10	25,347,618	25,347,687

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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