A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890635



Internal ID19184719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:817186..848643hg38UCSC Ensembl
Outerchr1:817186..848643hg38UCSC Ensembl
Innerchr1:752566..784023hg19UCSC Ensembl
Outerchr1:752566..784023hg19UCSC Ensembl
Innerchr1:742429..773886hg18UCSC Ensembl
Outerchr1:742429..773886hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3831458
hg1931458
hg1831458
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789091, essv25788744
Samples
Known GenesFAM87B, LINC00115, LINC01128
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890635
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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