A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797799



Internal ID19177276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:64436478..64473681hg38UCSC Ensembl
Innerchr5:63732305..63769508hg19UCSC Ensembl
Innerchr5:63768061..63805264hg18UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3837204
hg1937204
hg1837204
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894203
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797799
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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