A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1137201



Internal ID15643701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:72979640..73296530hg38UCSC Ensembl
Innerchr9:75594556..75911446hg19UCSC Ensembl
Innerchr9:74784376..75101266hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38316891
hg19316891
hg18316891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614612
Supporting Variants
Samples
Known GenesANXA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1137201
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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