A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18030130



Internal ID20597170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:5438379..5510341hg38UCSC Ensembl
chr16:5488380..5560342hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3871963
hg1971963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509890
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18030130
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00033


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