A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201819



Internal ID20768860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202089101..202105500hg38UCSC Ensembl
chr1:202058229..202074628hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3816400
hg1916400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332454
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201819
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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