A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890734



Internal ID19185036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:128897208..128953581hg38UCSC Ensembl
Outerchr5:128897208..128953581hg38UCSC Ensembl
Innerchr5:128232901..128289274hg19UCSC Ensembl
Outerchr5:128232901..128289274hg19UCSC Ensembl
Innerchr5:128260800..128317173hg18UCSC Ensembl
Outerchr5:128260800..128317173hg18UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg3856374
hg1956374
hg1856374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779246
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890734
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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