A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14243923



Internal ID21309478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:59042524..59094621hg38UCSC Ensembl
Outerchr11:59039768..59097071hg38UCSC Ensembl
Innerchr11:58809997..58862094hg19UCSC Ensembl
Outerchr11:58807241..58864544hg19UCSC Ensembl
Innerchr11:58566573..58618670hg18UCSC Ensembl
Outerchr11:58563817..58621120hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3857304
hg1957304
hg1857304
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169836
Supporting Variants
SamplesNGO_50
Known GenesLOC283194
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14243923
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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