A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247207



Internal ID21309626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4228783..4306942hg38UCSC Ensembl
Outerchr11:4217824..4314648hg38UCSC Ensembl
Innerchr11:4250013..4328172hg19UCSC Ensembl
Outerchr11:4239054..4335878hg19UCSC Ensembl
Innerchr11:4206589..4284748hg18UCSC Ensembl
Outerchr11:4195630..4292454hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3896825
hg1996825
hg1896825
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169696
Supporting Variants
SamplesNGO_51
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247207
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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