A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229200



Internal ID22371123
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14379100
SamplesNA19238
Known GenesVWA9
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229200
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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