A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594429



Internal ID21786472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82606369..82606369hg38UCSC Ensembl
chr11:82317411..82317411hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6089350
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594429
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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