A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14243072



Internal ID21310052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:59023521..59043770hg38UCSC Ensembl
Outerchr11:59011170..59043992hg38UCSC Ensembl
Innerchr11:58790994..58811243hg19UCSC Ensembl
Outerchr11:58778643..58811465hg19UCSC Ensembl
Innerchr11:58547570..58567819hg18UCSC Ensembl
Outerchr11:58535219..58568041hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3832823
hg1932823
hg1832823
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169836
Supporting Variants
SamplesNGO_54
Known GenesLOC283194
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14243072
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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