A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10752n54



Internal ID22778647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:67840103..67938976hg38UCSC Ensembl
chr6:68549996..68648868hg19UCSC Ensembl
chr6:68606717..68705589hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3898874
hg1998873
hg1898873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv603603, nsv603604
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10752n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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