A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025486



Internal ID84723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99084634..99098379hg38UCSC Ensembl
chr9:101846916..101860661hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3813746
hg1913746
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141967
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025486
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001093


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