A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5492n100



Internal ID22791579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184258978..184307462hg38UCSC Ensembl
chr4:185180131..185228615hg19UCSC Ensembl
chr4:185417125..185465609hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3848485
hg1948485
hg1848485
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021261, nsv1022143
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)dgv5492n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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