A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14241236



Internal ID21309421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93964770..93972107hg38UCSC Ensembl
Outerchr11:93959164..93974097hg38UCSC Ensembl
Innerchr11:93697936..93705273hg19UCSC Ensembl
Outerchr11:93692330..93707263hg19UCSC Ensembl
Innerchr11:93337584..93344921hg18UCSC Ensembl
Outerchr11:93331978..93346911hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3814934
hg1914934
hg1814934
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169868
Supporting Variants
SamplesNGO_5
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14241236
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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