A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18030983



Internal ID20598023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63687612..63702788hg38UCSC Ensembl
chr16:63721516..63736692hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3815177
hg1915177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509728
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18030983
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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