A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986419



Internal ID58381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111902790..111908895hg38UCSC Ensembl
chr6:112223993..112230098hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg386106
hg196106
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140844
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986419
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000343


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