A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12696n54



Internal ID22780591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62094726..62098994hg38UCSC Ensembl
chr9:40228515..40232782hg19UCSC Ensembl
chr9:40218515..40222782hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg384269
hg194268
hg184268
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614316, nsv614312, nsv614311, nsv614318, nsv614310, nsv614317, nsv614319, nsv614308, nsv614307, nsv614315, nsv614314
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12696n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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