A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12879n54



Internal ID20146303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127731234..127824409hg38UCSC Ensembl
chr9:130493513..130586688hg19UCSC Ensembl
chr9:129533334..129626509hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3893176
hg1993176
hg1893176
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615372, nsv615370
Samples1780862275_A
Known GenesCDK9, ENG, FPGS, MIR2861, MIR3960, SH2D3C, TOR2A, TTC16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12879n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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