A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10841n54



Internal ID22778736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:92821306..92897975hg38UCSC Ensembl
chr6:93531024..93607693hg19UCSC Ensembl
chr6:93587745..93664414hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3876670
hg1976670
hg1876670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604150, nsv604151
SamplesHGDP01087, HGDP00469
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10841n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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