A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185655



Internal ID20752695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85758635..85775358hg38UCSC Ensembl
chr16:85792241..85808964hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3816724
hg1916724
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511567
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185655
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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