A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893556



Internal ID19184376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:219779182..219795196hg38UCSC Ensembl
Outerchr2:219779182..219795196hg38UCSC Ensembl
Innerchr2:220643904..220659918hg19UCSC Ensembl
Outerchr2:220643904..220659918hg19UCSC Ensembl
Innerchr2:220352148..220368162hg18UCSC Ensembl
Outerchr2:220352148..220368162hg18UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3816015
hg1916015
hg1816015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784401
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893556
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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