A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778813



Internal ID19176274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:102139802..102186972hg38UCSC Ensembl
Innerchr5:101475506..101522676hg19UCSC Ensembl
Innerchr5:101503405..101550575hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3847171
hg1947171
hg1847171
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890685
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778813
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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