A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207192



Internal ID20774233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106662601..106670600hg38UCSC Ensembl
chr3:106381448..106389447hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371398
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207192
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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