A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031349



Internal ID20598389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67341081..67356360hg38UCSC Ensembl
chr16:67374984..67390263hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3815280
hg1915280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503948
Supporting Variants
Samples
Known GenesLRRC36
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031349
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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