A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025761



Internal ID84910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94335552..94348552hg38UCSC Ensembl
chr9:97097834..97110834hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3813001
hg1913001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142655
Supporting Variants
Samples
Known GenesLOC100132077
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025761
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00465


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