A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12887n54



Internal ID22780782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128689098..128690282hg38UCSC Ensembl
chr9:131451377..131452561hg19UCSC Ensembl
chr9:130491198..130492382hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381185
hg191185
hg181185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615409, nsv615406, nsv615407
Samples
Known GenesSET
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12887n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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