A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028602



Internal ID86768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124250520..124254964hg38UCSC Ensembl
chr9:127012799..127017243hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg384445
hg194445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487748
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028602
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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