A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615308



Internal ID16402717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126153569..126164710hg38UCSC Ensembl
Innerchr9:128915848..128926989hg19UCSC Ensembl
Innerchr9:127955669..127966810hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3811142
hg1911142
hg1811142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176493
SamplesHGDP00870
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615308
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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