A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890915



Internal ID19185311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:190952589..191053463hg38UCSC Ensembl
Outerchr1:190952589..191053463hg38UCSC Ensembl
Innerchr1:190921719..191022593hg19UCSC Ensembl
Outerchr1:190921719..191022593hg19UCSC Ensembl
Innerchr1:189188342..189289216hg18UCSC Ensembl
Outerchr1:189188342..189289216hg18UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38100875
hg19100875
hg18100875
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791321
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890915
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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