A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615606



Internal ID16056329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133078923..133155959hg38UCSC Ensembl
Innerchr9:135954310..136031346hg19UCSC Ensembl
Innerchr9:134944131..135021167hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3877037
hg1977037
hg1877037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12928n54
Supporting Variantsnssv1145396
Samples
Known GenesCELP, GBGT1, RALGDS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615606
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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