A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893768



Internal ID19184588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:80650955..80669238hg38UCSC Ensembl
Outerchr1:80650955..80669238hg38UCSC Ensembl
Innerchr1:81116640..81134923hg19UCSC Ensembl
Outerchr1:81116640..81134923hg19UCSC Ensembl
Innerchr1:80889228..80907511hg18UCSC Ensembl
Outerchr1:80889228..80907511hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3818284
hg1918284
hg1818284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779679
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893768
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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