A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031303



Internal ID20598343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66699457..66718973hg38UCSC Ensembl
chr16:66733360..66752876hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3819517
hg1919517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506306
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031303
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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