A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043539



Internal ID96749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60000..184000hg38UCSC Ensembl
chr11:60001..184000hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38124001
hg19124000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143272
Supporting Variants
Samples
Known GenesLINC01001
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043539
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000223


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