A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090975



Internal ID21491812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65581273..65581440hg38UCSC Ensembl
chr15:65873611..65873778hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585766
Supporting Variants
SamplesNA19238
Known GenesVWA9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090975
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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