A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199857



Internal ID20766897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:193797701..193895400hg38UCSC Ensembl
chr1:193766831..193864530hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg3897700
hg1997700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316581
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199857
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.03056


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