A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18030274



Internal ID20597314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3442670..3450668hg38UCSC Ensembl
chr16:3492670..3500668hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg387999
hg197999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513433
Supporting Variants
Samples
Known GenesNAA60, ZNF597
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18030274
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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