A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14246558



Internal ID21308535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:42948033..42949618hg38UCSC Ensembl
Outerchr11:42940281..42955081hg38UCSC Ensembl
Innerchr11:42969583..42971168hg19UCSC Ensembl
Outerchr11:42961831..42976631hg19UCSC Ensembl
Innerchr11:42926159..42927744hg18UCSC Ensembl
Outerchr11:42918407..42933207hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3814801
hg1914801
hg1814801
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169676
Supporting Variants
SamplesNGO_43
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14246558
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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