A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126921



Internal ID15633421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9796577..9819028hg38UCSC Ensembl
Innerchr9:9796577..9819028hg19UCSC Ensembl
Innerchr9:9786577..9809028hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3822452
hg1922452
hg1822452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613330
Supporting Variants
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1126921
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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