A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992719



Internal ID20559759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69526357..69528759hg38UCSC Ensembl
chr11:69341125..69343527hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg382403
hg192403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465021
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992719
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00028


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