A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893847



Internal ID19184667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192054084..192062743hg38UCSC Ensembl
Outerchr3:192054084..192062743hg38UCSC Ensembl
Innerchr3:191771873..191780532hg19UCSC Ensembl
Outerchr3:191771873..191780532hg19UCSC Ensembl
Innerchr3:193254567..193263226hg18UCSC Ensembl
Outerchr3:193254567..193263226hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg388660
hg198660
hg188660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780449
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893847
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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