A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029954



Internal ID20596994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:49125701..49176400hg38UCSC Ensembl
chr16:49159612..49210311hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3850700
hg1950700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514442
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029954
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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