A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614150



Internal ID16054873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33608617..33703236hg38UCSC Ensembl
Innerchr9:33608615..33703234hg19UCSC Ensembl
Innerchr9:33598615..33693234hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3894620
hg1994620
hg1894620
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132842
Samples
Known GenesANXA2P2, PTENP1, PTENP1-AS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614150
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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