A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799055



Internal ID19165539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55808492..55817065hg38UCSC Ensembl
Innerchr16:55842404..55850977hg19UCSC Ensembl
Innerchr16:54399905..54408478hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg388574
hg198574
hg188574
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892863
Supporting Variants
Samples
Known GenesCES1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799055
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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