A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12718n54



Internal ID22780613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67043898..67145229hg38UCSC Ensembl
chr9:43669753..43772166hg19UCSC Ensembl
chr9:43609749..43712162hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38101332
hg19102414
hg18102414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614430, nsv614435, nsv614427
Samples
Known GenesCNTNAP3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12718n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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