A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150102



Internal ID19199216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:65581248..65581441hg38UCSC Ensembl
Outerchr15:65873586..65873779hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998888
SamplesKWB1
Known GenesVWA9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150102
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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