A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893529



Internal ID19184349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:194855927..194953800hg38UCSC Ensembl
Outerchr2:194855927..194953800hg38UCSC Ensembl
Innerchr2:195720651..195818524hg19UCSC Ensembl
Outerchr2:195720651..195818524hg19UCSC Ensembl
Innerchr2:195428896..195526769hg18UCSC Ensembl
Outerchr2:195428896..195526769hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3897874
hg1997874
hg1897874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781590
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893529
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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