A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10256n54



Internal ID22778151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165391..253861hg38UCSC Ensembl
chr6:165391..253861hg19UCSC Ensembl
chr6:110391..198861hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3888471
hg1988471
hg1888471
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600738, nsv600739, nsv600735
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10256n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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