A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv160e55



Internal ID22761110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:117466188..117677028hg38UCSC Ensembl
chr2:118223764..118434604hg19UCSC Ensembl
chr2:117940234..118151074hg18UCSC Ensembl
chr2:117939994..118150834hg17UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg38210841
hg19210841
hg18210841
hg17210841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2751823, esv2751824
SamplesBEC_431, BEC_515
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv160e55
Frequency
Sample Size771
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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