A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779745



Internal ID19166379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:63152122..63233859hg38UCSC Ensembl
Innerchr5:62447949..62529686hg19UCSC Ensembl
Innerchr5:62483705..62565442hg18UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3881738
hg1981738
hg1881738
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894202
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779745
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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