A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9902n54



Internal ID22777797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82131900..82142325hg38UCSC Ensembl
chr5:81427719..81438144hg19UCSC Ensembl
chr5:81463475..81473900hg18UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg3810426
hg1910426
hg1810426
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv598762, nsv598765
Samples
Known GenesATG10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9902n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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