A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613202



Internal ID16400611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5602528..5634575hg38UCSC Ensembl
Innerchr9:5602528..5634575hg19UCSC Ensembl
Innerchr9:5592528..5624575hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3832048
hg1932048
hg1832048
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126531
Samples
Known GenesKIAA1432
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613202
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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