A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14251103



Internal ID21308509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:59042524..59086292hg38UCSC Ensembl
Outerchr11:59039768..59087546hg38UCSC Ensembl
Innerchr11:58809997..58853765hg19UCSC Ensembl
Outerchr11:58807241..58855019hg19UCSC Ensembl
Innerchr11:58566573..58610341hg18UCSC Ensembl
Outerchr11:58563817..58611595hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3847779
hg1947779
hg1847779
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169836
Supporting Variants
SamplesNGO_42
Known GenesLOC283194
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14251103
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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