A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989886



Internal ID20556926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35733317..35734025hg38UCSC Ensembl
chr11:35754865..35755573hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38709
hg19709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459658
Supporting Variants
Samples
Known GenesTRIM44
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989886
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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