A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12756n54



Internal ID22780651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73402591..73412434hg38UCSC Ensembl
chr9:76017507..76027350hg19UCSC Ensembl
chr9:75207327..75217170hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg389844
hg199844
hg189844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614652, nsv614651, nsv614649, nsv614646, nsv614637, nsv614636, nsv614653, nsv614645, nsv614643, nsv614644
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12756n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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