A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14379100



Internal ID22266174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65581273..65581441hg38UCSC Ensembl
chr15:65873611..65873779hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3229200
Supporting Variants
SamplesNA19238
Known GenesVWA9
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14379100
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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