A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979933



Internal ID54006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4492777..4518411hg38UCSC Ensembl
chr6:4493011..4518645hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3825635
hg1925635
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459745
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979933
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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