A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890687



Internal ID19184989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:103341663..103441319hg38UCSC Ensembl
Outerchr5:103341663..103441319hg38UCSC Ensembl
Innerchr5:102677364..102777020hg19UCSC Ensembl
Outerchr5:102677364..102777020hg19UCSC Ensembl
Innerchr5:102705263..102804919hg18UCSC Ensembl
Outerchr5:102705263..102804919hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3899657
hg1999657
hg1899657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799706
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890687
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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