A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208652



Internal ID20775694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41855905..42020299hg38UCSC Ensembl
chr3:41897397..42061791hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38164395
hg19164395
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359223
Supporting Variants
Samples
Known GenesULK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208652
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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