A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987852



Internal ID59337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107058552..107062312hg38UCSC Ensembl
chr6:107379756..107383516hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg383761
hg193761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469075
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987852
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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