A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16991386



Internal ID61671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170657100..170733796hg38UCSC Ensembl
chr6:170966188..171042884hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3876697
hg1976697
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142229
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16991386
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000639


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