A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979009



Internal ID53382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11161330..11166662hg38UCSC Ensembl
chr6:11161563..11166895hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg385333
hg195333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459973
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979009
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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