A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033048



Internal ID20600089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84706766..84731154hg38UCSC Ensembl
chr16:84740372..84764760hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3824389
hg1924389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502430
Supporting Variants
Samples
Known GenesUSP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033048
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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