A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787601



Internal ID19182797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:82346424..82561926hg38UCSC Ensembl
Innerchr2:82573548..82789050hg19UCSC Ensembl
Innerchr2:82427059..82642561hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38215503
hg19215503
hg18215503
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892825
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=39
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787601
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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