A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613613



Internal ID16054336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12641987..12773264hg38UCSC Ensembl
Innerchr9:12641987..12773263hg19UCSC Ensembl
Innerchr9:12631987..12763263hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38131278
hg19131277
hg18131277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1128716
Samples
Known GenesTYRP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613613
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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