A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074454



Internal ID20641494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44649780..44652187hg38UCSC Ensembl
chr22:45045660..45048067hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg382408
hg192408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536498
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074454
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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