A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14243238



Internal ID21311323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93964890..93968426hg38UCSC Ensembl
Outerchr11:93964792..93971294hg38UCSC Ensembl
Innerchr11:93698056..93701592hg19UCSC Ensembl
Outerchr11:93697958..93704460hg19UCSC Ensembl
Innerchr11:93337704..93341240hg18UCSC Ensembl
Outerchr11:93337606..93344108hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg386503
hg196503
hg186503
Variant TypeCNV deletion
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169868
Supporting Variants
SamplesSNI_1
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14243238
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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