A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028144



Internal ID86458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130084417..130084477hg38UCSC Ensembl
chr9:132846696..132846756hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485040
Supporting Variants
Samples
Known GenesGPR107
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028144
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.016089


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