A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10261n54



Internal ID22778156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:253861..394293hg38UCSC Ensembl
chr6:253861..394293hg19UCSC Ensembl
chr6:198861..339293hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38140433
hg19140433
hg18140433
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600752, nsv600748, nsv600749
SamplesHGDP00781, 1780854568_A, HGDP00330
Known GenesDUSP22, IRF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10261n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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