A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780057



Internal ID19168171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28763545..28824481hg38UCSC Ensembl
Innerchr5:28763652..28824588hg19UCSC Ensembl
Innerchr5:28799409..28860345hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3860937
hg1960937
hg1860937
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894161
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780057
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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