A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16995636



Internal ID64530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:49887468..49913412hg38UCSC Ensembl
chr7:49927064..49953008hg19UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg3825945
hg1925945
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474359
Supporting Variants
Samples
Known GenesVWC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16995636
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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