A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10626n54



Internal ID22778521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35534425..35594863hg38UCSC Ensembl
chr6:35502202..35562640hg19UCSC Ensembl
chr6:35610180..35670618hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3860439
hg1960439
hg1860439
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602921, nsv602922
SamplesHGDP00479, HGDP01262, HGDP00941
Known GenesFKBP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10626n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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