A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980525



Internal ID54398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34565287..34624523hg38UCSC Ensembl
chr6:34533064..34592300hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3859237
hg1959237
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455400
Supporting Variants
Samples
Known GenesC6orf106
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980525
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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