A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893780



Internal ID19184600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145585705..145639806hg38UCSC Ensembl
Outerchr3:145585705..145639806hg38UCSC Ensembl
Innerchr3:145303492..145357593hg19UCSC Ensembl
Outerchr3:145303492..145357593hg19UCSC Ensembl
Innerchr3:146786182..146840283hg18UCSC Ensembl
Outerchr3:146786182..146840283hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3854102
hg1954102
hg1854102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783665
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893780
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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