A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4140n100



Internal ID22790227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:192516979..192562183hg38UCSC Ensembl
chr2:193381705..193426909hg19UCSC Ensembl
chr2:193089950..193135154hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3845205
hg1945205
hg1845205
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009486, nsv1010559
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4140n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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