A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194732



Internal ID20761772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84133065..84181595hg38UCSC Ensembl
chr16:84166670..84215201hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3848531
hg1948532
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508726
Supporting Variants
Samples
Known GenesDNAAF1, HSDL1, TAF1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194732
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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