A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169574



Internal ID21313807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5864481..5914280hg38UCSC Ensembl
Outerchr11:5862087..5922193hg38UCSC Ensembl
Innerchr11:5885711..5935510hg19UCSC Ensembl
Outerchr11:5883317..5943423hg19UCSC Ensembl
Innerchr11:5842287..5892086hg18UCSC Ensembl
Outerchr11:5839893..5899999hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3860107
hg1960107
hg1860107
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247208, nssv14250313, nssv14242734, nssv14248254, nssv14250559, nssv14246877
SamplesNGO_3, NGO_27, NGO_9, NGO_4, MLY_2, NGO_6
Known GenesOR52E4
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169574
Frequency
Sample Size93
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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