A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18030242



Internal ID20597282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62129263..62166490hg38UCSC Ensembl
chr16:62163167..62200394hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3837228
hg1937228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514622
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18030242
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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