A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16988861



Internal ID60001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119641629..119698044hg38UCSC Ensembl
chr6:119962790..120019201hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3856416
hg1956412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473909
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16988861
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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