A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202332



Internal ID20769372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:199307317..199315447hg38UCSC Ensembl
chr1:199276445..199284575hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg388131
hg198131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327724
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202332
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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