A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893921



Internal ID18838089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:48950192..49089765hg38UCSC Ensembl
Outerchr4:48934804..49089765hg38UCSC Ensembl
Innerchr4:48952209..49091782hg19UCSC Ensembl
Outerchr4:48936821..49091782hg19UCSC Ensembl
Innerchr4:48646966..48786539hg18UCSC Ensembl
Outerchr4:48631578..48786539hg18UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg38154962
hg19154962
hg18154962
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788606, essv25788664
Samples
Known GenesCWH43
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893921
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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