A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580047



Internal ID21772090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5247795..5247795hg38UCSC Ensembl
chr11:5269025..5269025hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6090884
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580047
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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