A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027711



Internal ID86177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:119491798..119507526hg38UCSC Ensembl
chr9:122254076..122269804hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3815729
hg1915729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492115
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027711
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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