A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198733



Internal ID20765773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:104661446..104672293hg38UCSC Ensembl
chr1:105204068..105214915hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3810848
hg1910848
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331076
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198733
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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