A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788218



Internal ID19172578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:42427062..42492936hg38UCSC Ensembl
Innerchr11:42448612..42514486hg19UCSC Ensembl
Innerchr11:42405188..42471062hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3865875
hg1965875
hg1865875
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891969
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=20
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788218
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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