A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029827



Internal ID20596867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58373266..58424045hg38UCSC Ensembl
chr16:58407170..58457949hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3850780
hg1950780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501461
Supporting Variants
Samples
Known GenesGINS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029827
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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