A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986543



Internal ID58467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99519468..99524678hg38UCSC Ensembl
chr6:99967344..99972554hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg385211
hg195211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463951
Supporting Variants
Samples
Known GenesTSTD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986543
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001406


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