A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782885



Internal ID19176642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:12227022..12389639hg38UCSC Ensembl
Innerchr5:12227134..12389751hg19UCSC Ensembl
Innerchr5:12280134..12442751hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38162618
hg19162618
hg18162618
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894126
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782885
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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