A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613341



Internal ID16400750
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 StatusM
Merged Variantsdgv12505n54
Supporting Variantsnssv1126934
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613341
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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