A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893623



Internal ID19184443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:66756824..66797065hg38UCSC Ensembl
Outerchr1:66756824..66808318hg38UCSC Ensembl
Innerchr1:67222507..67262748hg19UCSC Ensembl
Outerchr1:67222507..67274001hg19UCSC Ensembl
Innerchr1:66995095..67035336hg18UCSC Ensembl
Outerchr1:66995095..67046589hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3851495
hg1951495
hg1851495
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787889, essv25788687, essv25787886
Samples
Known GenesINSL5, TCTEX1D1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893623
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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