A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12813n54



Internal ID22780708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101841564..101900303hg38UCSC Ensembl
chr9:104603846..104662585hg19UCSC Ensembl
chr9:103643667..103702406hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3858740
hg1958740
hg1858740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614972, nsv614971
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12813n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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