A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892024



Internal ID18839734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67768190..67820541hg38UCSC Ensembl
Outerchr11:67768190..67820541hg38UCSC Ensembl
Innerchr11:67535661..67588012hg19UCSC Ensembl
Outerchr11:67535661..67588012hg19UCSC Ensembl
Innerchr11:67292237..67344588hg18UCSC Ensembl
Outerchr11:67292237..67344588hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3852352
hg1952352
hg1852352
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781580
Samples
Known GenesFAM86C2P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892024
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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