A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14245391



Internal ID21306031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4234899..4286769hg38UCSC Ensembl
Outerchr11:4228783..4298482hg38UCSC Ensembl
Innerchr11:4256129..4307999hg19UCSC Ensembl
Outerchr11:4250013..4319712hg19UCSC Ensembl
Innerchr11:4212705..4264575hg18UCSC Ensembl
Outerchr11:4206589..4276288hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3869700
hg1969700
hg1869700
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169696
Supporting Variants
SamplesNGO_25
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14245391
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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