A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16981172



Internal ID54819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18326928..18331516hg38UCSC Ensembl
chr6:18327159..18331747hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384589
hg194589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463443
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16981172
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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