A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032213



Internal ID20599253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79617680..79617745hg38UCSC Ensembl
chr16:79651577..79651642hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508028
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032213
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0274


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