A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791718



Internal ID19174883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:106727587..106963579hg38UCSC Ensembl
Innerchr5:106063288..106299280hg19UCSC Ensembl
Innerchr5:106091187..106327179hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38235993
hg19235993
hg18235993
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890703
Supporting Variants
Samples
Known GenesLOC102467213
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=54
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791718
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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