A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785763



Internal ID19178055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:18768929..18970362hg38UCSC Ensembl
Innerchr5:18769038..18970471hg19UCSC Ensembl
Innerchr5:18804795..19006228hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38201434
hg19201434
hg18201434
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894148
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=46
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785763
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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