A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992469



Internal ID20559509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59853923..59854447hg38UCSC Ensembl
chr11:59621396..59621920hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38525
hg19525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468262
Supporting Variants
Samples
Known GenesTCN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992469
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01499


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