A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788245



Internal ID19179577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:60424580..60490975hg38UCSC Ensembl
Innerchr4:61290298..61356693hg19UCSC Ensembl
Innerchr4:60972893..61039288hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3866396
hg1966396
hg1866396
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893928
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788245
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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