A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14248706



Internal ID21307798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4228783..4325579hg38UCSC Ensembl
Outerchr11:4217824..4331751hg38UCSC Ensembl
Innerchr11:4250013..4346809hg19UCSC Ensembl
Outerchr11:4239054..4352981hg19UCSC Ensembl
Innerchr11:4206589..4303385hg18UCSC Ensembl
Outerchr11:4195630..4309557hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38113928
hg19113928
hg18113928
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169696
Supporting Variants
SamplesNGO_37
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14248706
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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