A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615612



Internal ID16056335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133156364..133290774hg38UCSC Ensembl
Innerchr9:136031751..136166346hg19UCSC Ensembl
Innerchr9:135021572..135156167hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38134411
hg19134596
hg18134596
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12930n54
Supporting Variantsnssv1176517
SamplesHGDP00545
Known GenesABO, GBGT1, OBP2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615612
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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