A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18031945



Internal ID20598985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71352616..71436646hg38UCSC Ensembl
chr16:71386519..71470549hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg3884031
hg1984031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504155
Supporting Variants
Samples
Known GenesCALB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18031945
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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