A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780859



Internal ID19164825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:60543296..60584144hg38UCSC Ensembl
Innerchr16:60577200..60618048hg19UCSC Ensembl
Innerchr16:59134701..59175549hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3840849
hg1940849
hg1840849
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892869
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780859
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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