A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890685



Internal ID19184987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:102139802..102186972hg38UCSC Ensembl
Outerchr5:102139802..102186972hg38UCSC Ensembl
Innerchr5:101475506..101522676hg19UCSC Ensembl
Outerchr5:101475506..101522676hg19UCSC Ensembl
Innerchr5:101503405..101550575hg18UCSC Ensembl
Outerchr5:101503405..101550575hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3847171
hg1947171
hg1847171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778813
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890685
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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