A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126934



Internal ID15980120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9803954..9832245hg38UCSC Ensembl
Innerchr9:9803954..9832245hg19UCSC Ensembl
Innerchr9:9793954..9822245hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3828292
hg1928292
hg1828292
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613341
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)nssv1126934
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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