A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033577



Internal ID20600617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86966624..86967102hg38UCSC Ensembl
chr16:87000230..87000708hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501433
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033577
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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