A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892825



Internal ID19183645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:82346424..82561926hg38UCSC Ensembl
Outerchr2:82346424..82561926hg38UCSC Ensembl
Innerchr2:82573548..82789050hg19UCSC Ensembl
Outerchr2:82573548..82789050hg19UCSC Ensembl
Innerchr2:82427059..82642561hg18UCSC Ensembl
Outerchr2:82427059..82642561hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38215503
hg19215503
hg18215503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787601
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892825
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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