A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4914n100



Internal ID22791001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:144056516..144149508hg38UCSC Ensembl
chr3:143775358..143868350hg19UCSC Ensembl
chr3:145258048..145351040hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3892993
hg1992993
hg1892993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010213, nsv1009018
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4914n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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