A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615602



Internal ID16056325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133073855..133080439hg38UCSC Ensembl
Innerchr9:135949242..135955826hg19UCSC Ensembl
Innerchr9:134939063..134945647hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg386585
hg196585
hg186585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12926n54
Supporting Variantsnssv1145390
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615602
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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