A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1279n54



Internal ID22769174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79376259..79424128hg38UCSC Ensembl
chr10:81136015..81183884hg19UCSC Ensembl
chr10:80806021..80853890hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3847870
hg1947870
hg1847870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551587, nsv551586
SamplesNINDS_49
Known GenesZCCHC24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1279n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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