A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033383



Internal ID20600423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85447147..85447564hg38UCSC Ensembl
chr16:85480753..85481170hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496508
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033383
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00066


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