A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027120



Internal ID85800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122769578..122769581hg38UCSC Ensembl
chr9:125531857..125531860hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5552893
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027120
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.005308


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