A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25793000



Internal ID19176351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167283413..167343098hg38UCSC Ensembl
Innerchr4:168204564..168264249hg19UCSC Ensembl
Innerchr4:168441139..168500824hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3859686
hg1959686
hg1859686
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894068
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25793000
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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