A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202411



Internal ID20769451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235105980..235106704hg38UCSC Ensembl
chr1:235269295..235270019hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg38725
hg19725
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318085
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202411
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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