A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185729



Internal ID20752769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56160871..56261662hg38UCSC Ensembl
chr18:53828102..53928893hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38100792
hg19100792
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526290
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185729
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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