A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993747



Internal ID20560787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58557167..58557639hg38UCSC Ensembl
chr11:58324640..58325112hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38473
hg19473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471298
Supporting Variants
Samples
Known GenesLPXN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993747
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00142


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