A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5326n100



Internal ID22791413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77260884..77396686hg38UCSC Ensembl
chr4:78182037..78317840hg19UCSC Ensembl
chr4:78401061..78536864hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38135803
hg19135804
hg18135804
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004824, nsv1000447, nsv1010450
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)dgv5326n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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