A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613738



Internal ID16401147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20005314..20287950hg38UCSC Ensembl
Innerchr9:20005312..20287948hg19UCSC Ensembl
Innerchr9:19995312..20277948hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38282637
hg19282637
hg18282637
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156450
Samples1780862339_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613738
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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