A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893827



Internal ID18837961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:179207079..179304740hg38UCSC Ensembl
Outerchr3:179207079..179304740hg38UCSC Ensembl
Innerchr3:178924867..179022528hg19UCSC Ensembl
Outerchr3:178924867..179022528hg19UCSC Ensembl
Innerchr3:180407561..180505222hg18UCSC Ensembl
Outerchr3:180407561..180505222hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3897662
hg1997662
hg1897662
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792709
Samples
Known GenesKCNMB3, PIK3CA
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893827
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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