A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189741



Internal ID20756781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28217923..28240835hg38UCSC Ensembl
chr16:28229244..28252156hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3822913
hg1922913
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507284
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189741
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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