A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10926n54



Internal ID22778821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125860810..125865498hg38UCSC Ensembl
chr6:126181956..126186644hg19UCSC Ensembl
chr6:126223649..126228337hg18UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg384689
hg194689
hg184689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604606, nsv604604, nsv604605
Samples
Known GenesNCOA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10926n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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