A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990561



Internal ID61121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164268086..164271155hg38UCSC Ensembl
chr6:164689119..164692188hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg383070
hg193070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463787
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990561
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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