A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14245500



Internal ID21309040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:59042524..59087573hg38UCSC Ensembl
Outerchr11:59039768..59091425hg38UCSC Ensembl
Innerchr11:58809997..58855046hg19UCSC Ensembl
Outerchr11:58807241..58858898hg19UCSC Ensembl
Innerchr11:58566573..58611622hg18UCSC Ensembl
Outerchr11:58563817..58615474hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3851658
hg1951658
hg1851658
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169836
Supporting Variants
SamplesNGO_47
Known GenesLOC283194
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14245500
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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