A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169911



Internal ID21313722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:79993724..80021445hg38UCSC Ensembl
Outerchr11:79992597..80024312hg38UCSC Ensembl
Innerchr11:79704767..79732488hg19UCSC Ensembl
Outerchr11:79703640..79735355hg19UCSC Ensembl
Innerchr11:79382415..79410136hg18UCSC Ensembl
Outerchr11:79381288..79413003hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3831716
hg1931716
hg1831716
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14248857
SamplesMLY_12
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169911
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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