A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071890



Internal ID20638930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31301119..31318917hg38UCSC Ensembl
chr21:32673434..32691232hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3817799
hg1917799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538742
Supporting Variants
Samples
Known GenesTIAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071890
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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