A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893736



Internal ID19184556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:84567113..84747499hg38UCSC Ensembl
Outerchr3:84567113..84747499hg38UCSC Ensembl
Innerchr3:84616264..84796650hg19UCSC Ensembl
Outerchr3:84616264..84796650hg19UCSC Ensembl
Innerchr3:84698954..84879340hg18UCSC Ensembl
Outerchr3:84698954..84879340hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38180387
hg19180387
hg18180387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791459
Samples
Known GenesLINC00971
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893736
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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