A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992726



Internal ID20559766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69688384..69689544hg38UCSC Ensembl
chr11:69503152..69504312hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg381161
hg191161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471673
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992726
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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