A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5323n100



Internal ID22791410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77236374..77360177hg38UCSC Ensembl
chr4:78157527..78281331hg19UCSC Ensembl
chr4:78376551..78500355hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38123804
hg19123805
hg18123805
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv998039, nsv1009917, nsv1002683, nsv1011073, nsv1003383, nsv1014839, nsv1014450, nsv1003098
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)dgv5323n100
Frequency
Sample Size11257
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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