A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989366



Internal ID60335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151597957..151644772hg38UCSC Ensembl
chr6:151919092..151965907hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3846816
hg1946816
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5456081
Supporting Variants
Samples
Known GenesCCDC170
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989366
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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