A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14252291



Internal ID21303340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38301195..38340379hg38UCSC Ensembl
Outerchr11:38298562..38348573hg38UCSC Ensembl
Innerchr11:38322745..38361929hg19UCSC Ensembl
Outerchr11:38320112..38370123hg19UCSC Ensembl
Innerchr11:38279321..38318505hg18UCSC Ensembl
Outerchr11:38276688..38326699hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3850012
hg1950012
hg1850012
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169556
Supporting Variants
SamplesMLY_5
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14252291
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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