A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987699



Internal ID59241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117709121..117709250hg38UCSC Ensembl
chr6:118030284..118030413hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462477
Supporting Variants
Samples
Known GenesNUS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987699
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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