A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5322n100



Internal ID22791409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77199719..77339116hg38UCSC Ensembl
chr4:78120872..78260269hg19UCSC Ensembl
chr4:78339896..78479293hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38139398
hg19139398
hg18139398
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1014055, nsv998972, nsv1014305, nsv1007726, nsv1010406, nsv1003755, nsv1001852, nsv1012298
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)dgv5322n100
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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