A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14243766



Internal ID21310171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4228783..4338058hg38UCSC Ensembl
Outerchr11:4217824..4363567hg38UCSC Ensembl
Innerchr11:4250013..4359288hg19UCSC Ensembl
Outerchr11:4239054..4384797hg19UCSC Ensembl
Innerchr11:4206589..4315864hg18UCSC Ensembl
Outerchr11:4195630..4341373hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38145744
hg19145744
hg18145744
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169696
Supporting Variants
SamplesNGO_55
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14243766
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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