A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10865n54



Internal ID22778760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:100611010..100750077hg38UCSC Ensembl
chr6:101058886..101197953hg19UCSC Ensembl
chr6:101165607..101304674hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38139068
hg19139068
hg18139068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604273, nsv604270, nsv604274, nsv604272
Samples
Known GenesASCC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10865n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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