A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615150



Internal ID16055873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:110067939..110096621hg38UCSC Ensembl
Innerchr9:112830219..112858901hg19UCSC Ensembl
Innerchr9:111870040..111898722hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3828683
hg1928683
hg1828683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176114
SamplesHGDP01417
Known GenesAKAP2, PALM2-AKAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615150
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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