A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12695n54



Internal ID22780590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67330186..67423306hg38UCSC Ensembl
chr9:40064995..40162120hg19UCSC Ensembl
chr9:40054995..40152120hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3893121
hg1997126
hg1897126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614304, nsv614303
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12695n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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