A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614730



Internal ID16055453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77447358..77472115hg38UCSC Ensembl
Innerchr9:80062274..80087031hg19UCSC Ensembl
Innerchr9:79252094..79276851hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3824758
hg1924758
hg1824758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1137701
Samples
Known GenesGNA14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614730
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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