A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16988151



Internal ID59527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:120660000..120691000hg38UCSC Ensembl
chr6:120981146..121012146hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3831001
hg1931001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466007
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16988151
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000469


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