A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893760



Internal ID19184580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:109765455..110087876hg38UCSC Ensembl
Outerchr3:109765455..110087876hg38UCSC Ensembl
Innerchr3:109484302..109806723hg19UCSC Ensembl
Outerchr3:109484302..109806723hg19UCSC Ensembl
Innerchr3:110966992..111289413hg18UCSC Ensembl
Outerchr3:110966992..111289413hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38322422
hg19322422
hg18322422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780441
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893760
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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