A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv13006n54



Internal ID22780901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136619086..136725859hg38UCSC Ensembl
chr9:139513538..139620311hg19UCSC Ensembl
chr9:138633359..138740132hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38106774
hg19106774
hg18106774
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv615978, nsv615981
Samples1780862388_A, 1780862100_A
Known GenesAGPAT2, EGFL7, FAM69B, MIR126, SNHG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv13006n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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