A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890669



Internal ID19184971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:90347582..90358360hg38UCSC Ensembl
Outerchr5:90347582..90358360hg38UCSC Ensembl
Innerchr5:89643399..89654177hg19UCSC Ensembl
Outerchr5:89643399..89654177hg19UCSC Ensembl
Innerchr5:89679155..89689933hg18UCSC Ensembl
Outerchr5:89679155..89689933hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3810779
hg1910779
hg1810779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779035
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890669
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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