A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8196n54



Internal ID22776091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:6583394..6612373hg38UCSC Ensembl
chr3:6625081..6654060hg19UCSC Ensembl
chr3:6600081..6629060hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3828980
hg1928980
hg1828980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589525, nsv589524
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8196n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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