A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891924



Internal ID19186320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6972691..6991683hg38UCSC Ensembl
Outerchr11:6972691..6991683hg38UCSC Ensembl
Innerchr11:6993922..7012914hg19UCSC Ensembl
Outerchr11:6993922..7012914hg19UCSC Ensembl
Innerchr11:6950498..6969490hg18UCSC Ensembl
Outerchr11:6950498..6969490hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3818993
hg1918993
hg1818993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785807
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891924
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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