A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782360



Internal ID19174632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9583646..9635292hg38UCSC Ensembl
Innerchr16:9677503..9729149hg19UCSC Ensembl
Innerchr16:9585004..9636650hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3851647
hg1951647
hg1851647
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892789
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782360
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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