A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893559



Internal ID19184379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:220744041..220773560hg38UCSC Ensembl
Outerchr2:220744041..220773560hg38UCSC Ensembl
Innerchr2:221608761..221638280hg19UCSC Ensembl
Outerchr2:221608761..221638280hg19UCSC Ensembl
Innerchr2:221317005..221346524hg18UCSC Ensembl
Outerchr2:221317005..221346524hg18UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg3829520
hg1929520
hg1829520
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781798
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893559
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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