A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247874



Internal ID21311764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4251190..4298484hg38UCSC Ensembl
Outerchr11:4248034..4306942hg38UCSC Ensembl
Innerchr11:4272420..4319714hg19UCSC Ensembl
Outerchr11:4269264..4328172hg19UCSC Ensembl
Innerchr11:4228996..4276290hg18UCSC Ensembl
Outerchr11:4225840..4284748hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3858909
hg1958909
hg1858909
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169696
Supporting Variants
SamplesSNI_13
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247874
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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