A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792547



Internal ID19178276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41782346..41818990hg38UCSC Ensembl
Innerchr3:41823838..41860482hg19UCSC Ensembl
Innerchr3:41798842..41835486hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3836645
hg1936645
hg1836645
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893689
Supporting Variants
Samples
Known GenesULK4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792547
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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