A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208531



Internal ID20775572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:165799619..166157754hg38UCSC Ensembl
chr3:165517407..165875542hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38358136
hg19358136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357577
Supporting Variants
Samples
Known GenesBCHE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208531
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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