A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12506n54



Internal ID22780401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:9793342..9869714hg38UCSC Ensembl
chr9:9793342..9869714hg19UCSC Ensembl
chr9:9783342..9859714hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3876373
hg1976373
hg1876373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613343, nsv613338, nsv613327, nsv613342, nsv613346, nsv613337, nsv613344, nsv613332, nsv613326
Samples1780862088_A
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12506n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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