A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5192n100



Internal ID22791279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38462872..38540841hg38UCSC Ensembl
chr4:38464493..38542462hg19UCSC Ensembl
chr4:38140888..38218857hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3877970
hg1977970
hg1877970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004725, nsv998791
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)dgv5192n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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