A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986968



Internal ID58762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:97406790..97452790hg38UCSC Ensembl
chr6:97854666..97900666hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3846001
hg1946001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464382
Supporting Variants
Samples
Known GenesMIR548H3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986968
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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