A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894181



Internal ID19185250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:41222684..41234906hg38UCSC Ensembl
Outerchr5:41222684..41234906hg38UCSC Ensembl
Innerchr5:41222786..41235008hg19UCSC Ensembl
Outerchr5:41222786..41235008hg19UCSC Ensembl
Innerchr5:41258543..41270765hg18UCSC Ensembl
Outerchr5:41258543..41270765hg18UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3812223
hg1912223
hg1812223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784849, essv25783554, essv25800338
Samples
Known GenesC6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894181
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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