A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178552



Internal ID20745592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74977485..74988565hg38UCSC Ensembl
chr16:75011383..75022463hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3811081
hg1911081
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497683
Supporting Variants
Samples
Known GenesWDR59
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178552
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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