A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615392



Internal ID16056115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128663931..128690219hg38UCSC Ensembl
Innerchr9:131426210..131452498hg19UCSC Ensembl
Innerchr9:130466031..130492319hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3826289
hg1926289
hg1826289
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12882n54
Supporting Variantsnssv1143223
Samples
Known GenesSET
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615392
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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