A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204150



Internal ID20771190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44748501..44751100hg38UCSC Ensembl
chr21:46168416..46171015hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536886
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204150
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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