A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12716n54



Internal ID22780611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67036224..67163322hg38UCSC Ensembl
chr9:43659129..43790296hg19UCSC Ensembl
chr9:43599125..43730292hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38127099
hg19131168
hg18131168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614423, nsv614436, nsv614422, nsv614434, nsv614424
Samples
Known GenesCNTNAP3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12716n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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