A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614324



Internal ID16401733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:66775716..66902361hg38UCSC Ensembl
Innerchr9:40790480..40917166hg19UCSC Ensembl
Innerchr9:40780480..40907166hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38126646
hg19126687
hg18126687
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1134155
Samples
Known GenesZNF658
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614324
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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