A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033808



Internal ID20600848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89740717..89801784hg38UCSC Ensembl
chr16:89807125..89868192hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3861068
hg1961068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513968
Supporting Variants
Samples
Known GenesFANCA, ZNF276
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033808
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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