A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10984n54



Internal ID22778879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157671606..157694755hg38UCSC Ensembl
chr6:158092638..158115787hg19UCSC Ensembl
chr6:158012626..158035775hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3823150
hg1923150
hg1823150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604978, nsv604979
SamplesHGDP00830
Known GenesZDHHC14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10984n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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