A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5496n100



Internal ID20157112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:187167070..188594145hg38UCSC Ensembl
chr4:188088224..189515299hg19UCSC Ensembl
chr4:188325218..189752293hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381427076
hg191427076
hg181427076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018893, nsv1029769, nsv1028007
Samples
Known GenesLINC01060, LOC339975, TRIML1, TRIML2, ZFP42
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5496n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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