A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892049



Internal ID18839759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85977166..85992931hg38UCSC Ensembl
Outerchr11:85977166..85992931hg38UCSC Ensembl
Innerchr11:85688209..85703974hg19UCSC Ensembl
Outerchr11:85688209..85703974hg19UCSC Ensembl
Innerchr11:85365857..85381622hg18UCSC Ensembl
Outerchr11:85365857..85381622hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3815766
hg1915766
hg1815766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786896
Samples
Known GenesPICALM
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892049
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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