A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10727n54



Internal ID22778622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:65427367..65522799hg38UCSC Ensembl
chr6:66137260..66232692hg19UCSC Ensembl
chr6:66193981..66289413hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3895433
hg1995433
hg1895433
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv603440, nsv603441
SamplesHGDP00146
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10727n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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