A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5003n100



Internal ID22791090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186668758..186709255hg38UCSC Ensembl
chr3:186386547..186427044hg19UCSC Ensembl
chr3:187869241..187909738hg18UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3840498
hg1940498
hg1840498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007403, nsv1008812, nsv1004787, nsv1014443
Samples
Known GenesHRG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5003n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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