A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615597



Internal ID16056320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133061291..133080439hg38UCSC Ensembl
Innerchr9:135936678..135955826hg19UCSC Ensembl
Innerchr9:134926499..134945647hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3819149
hg1919149
hg1819149
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12925n54
Supporting Variantsnssv1145381
Samples
Known GenesCEL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615597
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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