A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209211



Internal ID20776251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170673801..170684500hg38UCSC Ensembl
chr3:170391590..170402289hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3810700
hg1910700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362585
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209211
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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