A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12891n54



Internal ID22780786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129377690..129419493hg38UCSC Ensembl
chr9:132139969..132181772hg19UCSC Ensembl
chr9:131179790..131221593hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3841804
hg1941804
hg1841804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615424, nsv615425, nsv615428
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12891n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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