A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191896



Internal ID20758936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48445715..48529027hg38UCSC Ensembl
chr18:45972086..46055398hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3883313
hg1983313
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528709
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191896
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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