A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615151



Internal ID16055874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:110157008..110175898hg38UCSC Ensembl
Innerchr9:112919288..112938178hg19UCSC Ensembl
Innerchr9:111959109..111977999hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3818891
hg1918891
hg1818891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176115
SamplesHGDP00925
Known GenesAKAP2, PALM2-AKAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615151
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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