A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800084



Internal ID19173633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128092144..128116307hg38UCSC Ensembl
Innerchr11:127962039..127986202hg19UCSC Ensembl
Innerchr11:127467249..127491412hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3824164
hg1924164
hg1824164
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892107
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800084
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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