A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782103



Internal ID19175031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58864281..58879946hg38UCSC Ensembl
Innerchr16:58898185..58913850hg19UCSC Ensembl
Innerchr16:57455686..57471351hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3815666
hg1915666
hg1815666
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892866
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782103
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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