A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786537



Internal ID19165923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:114731524..114809224hg38UCSC Ensembl
Innerchr5:114067221..114144921hg19UCSC Ensembl
Innerchr5:114095120..114172820hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3877701
hg1977701
hg1877701
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890714
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786537
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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