A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196945



Internal ID20763985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:53832735..53886144hg38UCSC Ensembl
chr18:51359105..51412514hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3853410
hg1953410
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522523
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196945
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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