A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208495



Internal ID20775536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128662001..128684600hg38UCSC Ensembl
chr3:128380844..128403443hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3822600
hg1922600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371667
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208495
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.02742


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