A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028045



Internal ID86391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129043837..129044063hg38UCSC Ensembl
chr9:131806116..131806342hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485215
Supporting Variants
Samples
Known GenesFAM73B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028045
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


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