A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8176n54



Internal ID22776071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4034049..4062242hg38UCSC Ensembl
chr3:4075733..4103926hg19UCSC Ensembl
chr3:4050733..4078926hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3828194
hg1928194
hg1828194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589413, nsv589412
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8176n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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