A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8180n54



Internal ID20141604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4087093..4124049hg38UCSC Ensembl
chr3:4128777..4165733hg19UCSC Ensembl
chr3:4103777..4140733hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3836957
hg1936957
hg1836957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589432, nsv589430, nsv589429
SamplesHGDP00279
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8180n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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