A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787859



Internal ID19172959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180667042..180763328hg38UCSC Ensembl
Innerchr5:180094042..180190328hg19UCSC Ensembl
Innerchr5:180026648..180122934hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3896287
hg1996287
hg1896287
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890776
Supporting Variants
Samples
Known GenesOR2Y1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=24
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787859
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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