A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028571



Internal ID20595611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26172101..26177700hg38UCSC Ensembl
chr16:26183422..26189021hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504497
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028571
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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