A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979191



Internal ID53507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17347806..17348539hg38UCSC Ensembl
chr6:17348037..17348770hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459430
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979191
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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