A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10263n54



Internal ID22778158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:274847..390105hg38UCSC Ensembl
chr6:274847..390105hg19UCSC Ensembl
chr6:219847..335105hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38115259
hg19115259
hg18115259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600763, nsv600762, nsv600756, nsv600757, nsv600760
SamplesHGDP01288, HGDP00801, HGDP00701
Known GenesDUSP22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10263n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer