A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17991382



Internal ID20558422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4393001..4394600hg38UCSC Ensembl
chr11:4414231..4415830hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449089
Supporting Variants
Samples
Known GenesTRIM21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17991382
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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