A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12794n54



Internal ID22780689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91640037..91641031hg38UCSC Ensembl
chr9:94402319..94403313hg19UCSC Ensembl
chr9:93442140..93443134hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38995
hg19995
hg18995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614876, nsv614875, nsv614874
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12794n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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