A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031907



Internal ID20598947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:70575359..70577849hg38UCSC Ensembl
chr16:70609262..70611752hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382491
hg192491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502189
Supporting Variants
Samples
Known GenesSF3B3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031907
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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