A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10410n54



Internal ID22778305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31314218..31371463hg38UCSC Ensembl
chr6:31281995..31339240hg19UCSC Ensembl
chr6:31389974..31447219hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3857246
hg1957246
hg1857246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601668, nsv601686
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)dgv10410n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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