A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10440n54



Internal ID22778335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31343568..31372094hg38UCSC Ensembl
chr6:31311345..31339871hg19UCSC Ensembl
chr6:31419324..31447850hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3828527
hg1928527
hg1828527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601825, nsv601827, nsv601826
Samples
Known GenesHLA-B, MIR6891
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10440n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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