A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792978



Internal ID19175714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163176035..163258345hg38UCSC Ensembl
Innerchr3:162893823..162976133hg19UCSC Ensembl
Innerchr3:164376517..164458827hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3882311
hg1982311
hg1882311
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893803
Supporting Variants
Samples
Known GenesCT64
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=17
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792978
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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