A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589555



Internal ID21781598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128954300..128954467hg38UCSC Ensembl
chr9:131716579..131716746hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6010049
Supporting Variants
Samples
Known GenesNUP188
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589555
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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