A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10e55



Internal ID22760960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:193694146..193741066hg38UCSC Ensembl
chr1:193663276..193710196hg19UCSC Ensembl
chr1:191929899..191976819hg18UCSC Ensembl
chr1:190394933..190441853hg17UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg3846921
hg1946921
hg1846921
hg1746921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv34863, esv34261
SamplesNA19209, NA19154
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)dgv10e55
Frequency
Sample Size771
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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