A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12526n54



Internal ID22780421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11619839..11835471hg38UCSC Ensembl
chr9:11619839..11835471hg19UCSC Ensembl
chr9:11609839..11825471hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38215633
hg19215633
hg18215633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613434, nsv613440
Samples1798860336_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12526n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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