A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992437



Internal ID20559477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59344998..59351629hg38UCSC Ensembl
chr11:59112471..59119102hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg386632
hg196632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6469593
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992437
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00306


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