A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203933



Internal ID20770973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:35882701..35905800hg38UCSC Ensembl
chr21:37254999..37278098hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3823100
hg1923100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544297
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203933
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00087


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