A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5290n100



Internal ID22791377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68725894..68802278hg38UCSC Ensembl
chr4:69591612..69667996hg19UCSC Ensembl
chr4:69626201..69702585hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3876385
hg1976385
hg1876385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1014042, nsv1013885
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)dgv5290n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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