A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14246877



Internal ID21302865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5864479..5914280hg38UCSC Ensembl
Outerchr11:5862087..5922193hg38UCSC Ensembl
Innerchr11:5885709..5935510hg19UCSC Ensembl
Outerchr11:5883317..5943423hg19UCSC Ensembl
Innerchr11:5842285..5892086hg18UCSC Ensembl
Outerchr11:5839893..5899999hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3860107
hg1960107
hg1860107
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169574
Supporting Variants
SamplesMLY_2
Known GenesOR52E4
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14246877
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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