A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022090



Internal ID82390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:29200346..29200542hg38UCSC Ensembl
chr9:29200344..29200540hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489224
Supporting Variants
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022090
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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