A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10661n54



Internal ID20144085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52748261..52809153hg38UCSC Ensembl
chr6:52613059..52673951hg19UCSC Ensembl
chr6:52721018..52781910hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3860893
hg1960893
hg1860893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv603108, nsv603107
Samples
Known GenesGSTA1, GSTA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10661n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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