A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613015



Internal ID16400424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:438295..484850hg38UCSC Ensembl
Innerchr9:438295..484850hg19UCSC Ensembl
Innerchr9:428295..474850hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3846556
hg1946556
hg1846556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1125978
Samples
Known GenesDOCK8, KANK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613015
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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