A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615426



Internal ID16402835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129384126..129400174hg38UCSC Ensembl
Innerchr9:132146405..132162453hg19UCSC Ensembl
Innerchr9:131186226..131202274hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3816049
hg1916049
hg1816049
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176149
SamplesHGDP00833
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615426
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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