A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196539



Internal ID20763579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:30484269..30502671hg38UCSC Ensembl
chr18:28064235..28082637hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3818403
hg1918403
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517428
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196539
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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