A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025397



Internal ID84665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83627049..83627130hg38UCSC Ensembl
chr9:86241964..86242045hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490829
Supporting Variants
Samples
Known GenesIDNK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025397
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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