A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790749



Internal ID19179868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84058861..84081674hg38UCSC Ensembl
Innerchr16:84092466..84115279hg19UCSC Ensembl
Innerchr16:82649967..82672780hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3822814
hg1922814
hg1822814
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892927
Supporting Variants
Samples
Known GenesMBTPS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790749
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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