A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613204



Internal ID16400613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5931216..5971977hg38UCSC Ensembl
Innerchr9:5931216..5971977hg19UCSC Ensembl
Innerchr9:5921216..5961977hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3840762
hg1940762
hg1840762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126533
Samples
Known GenesKIAA2026
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613204
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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