A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615617



Internal ID16056340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133255902..133257230hg38UCSC Ensembl
Innerchr9:136131289..136132617hg19UCSC Ensembl
Innerchr9:135121110..135122438hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg381329
hg191329
hg181329
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1145404
Samples
Known GenesABO
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615617
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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