A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893802



Internal ID19184622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162908797..163207950hg38UCSC Ensembl
Outerchr3:162908797..163207950hg38UCSC Ensembl
Innerchr3:162626585..162925738hg19UCSC Ensembl
Outerchr3:162626585..162925738hg19UCSC Ensembl
Innerchr3:164109279..164408432hg18UCSC Ensembl
Outerchr3:164109279..164408432hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38299154
hg19299154
hg18299154
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789193
Samples
Known GenesCT64
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893802
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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