A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247441



Internal ID21306533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4946883..4955852hg38UCSC Ensembl
Outerchr11:4946420..4957152hg38UCSC Ensembl
Innerchr11:4968113..4977082hg19UCSC Ensembl
Outerchr11:4967650..4978382hg19UCSC Ensembl
Innerchr11:4924689..4933658hg18UCSC Ensembl
Outerchr11:4924226..4934958hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3810733
hg1910733
hg1810733
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170219
Supporting Variants
SamplesNGO_28
Known GenesOR51A2, OR51A4
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247441
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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