A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1128508



Internal ID15981694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10421687..10495679hg38UCSC Ensembl
Innerchr9:10421687..10495679hg19UCSC Ensembl
Innerchr9:10411687..10485679hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3873993
hg1973993
hg1873993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613384
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)nssv1128508
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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