A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008965



Internal ID20576007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41731654..41732258hg38UCSC Ensembl
chr13:42305790..42306394hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6476425
Supporting Variants
Samples
Known GenesVWA8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008965
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00037


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