A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224270



Internal ID20791310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18544059..18663292hg38UCSC Ensembl
chr8:18401569..18520802hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38119234
hg19119234
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418900
Supporting Variants
Samples
Known GenesPSD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224270
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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