A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1128716



Internal ID15635216
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 StatusS
Merged Variantsnsv613613
Supporting Variants
Samples
Known GenesTYRP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1128716
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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