A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890701



Internal ID19185003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:106077397..106233242hg38UCSC Ensembl
Outerchr5:106077397..106233242hg38UCSC Ensembl
Innerchr5:105413098..105568943hg19UCSC Ensembl
Outerchr5:105413098..105568943hg19UCSC Ensembl
Innerchr5:105440997..105596842hg18UCSC Ensembl
Outerchr5:105440997..105596842hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38155846
hg19155846
hg18155846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787675
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890701
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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