A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17593385



Internal ID21785428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111591129..111591219hg38UCSC Ensembl
chr9:114353409..114353499hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017494
Supporting Variants
Samples
Known GenesPTGR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17593385
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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