A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198728



Internal ID20765768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:104409517..104492080hg38UCSC Ensembl
chr1:104952139..105034702hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3882564
hg1982564
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331450
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198728
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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