A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892078



Internal ID19186474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96785453..96854720hg38UCSC Ensembl
Outerchr11:96782321..96855926hg38UCSC Ensembl
Innerchr11:96656453..96725720hg19UCSC Ensembl
Outerchr11:96653321..96726926hg19UCSC Ensembl
Innerchr11:96161663..96230930hg18UCSC Ensembl
Outerchr11:96158531..96232136hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3873606
hg1973606
hg1873606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786348, essv25783333, essv25782032, essv25797461
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892078
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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