A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893901



Internal ID19184755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:104414941..104449028hg38UCSC Ensembl
Outerchr1:104387864..104454849hg38UCSC Ensembl
Innerchr1:104957563..104991650hg19UCSC Ensembl
Outerchr1:104930486..104997471hg19UCSC Ensembl
Innerchr1:104759086..104793173hg18UCSC Ensembl
Outerchr1:104732009..104798994hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3866986
hg1966986
hg1866986
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787858, essv25792257, essv25788293, essv25793032
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893901
Frequency
Sample Size3017
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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