A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980903



Internal ID54639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28863584..28863668hg38UCSC Ensembl
chr6:28831361..28831445hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467914
Supporting Variants
Samples
Known GenesLOC401242
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980903
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002029


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