A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893525



Internal ID19184345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:193405174..193574366hg38UCSC Ensembl
Outerchr2:193405174..193574366hg38UCSC Ensembl
Innerchr2:194269899..194439091hg19UCSC Ensembl
Outerchr2:194269899..194439091hg19UCSC Ensembl
Innerchr2:193978144..194147336hg18UCSC Ensembl
Outerchr2:193978144..194147336hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38169193
hg19169193
hg18169193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785597
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893525
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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