A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032755



Internal ID20599795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75924898..75997761hg38UCSC Ensembl
chr16:75958796..76031659hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3872864
hg1972864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496907
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032755
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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