A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588813



Internal ID21780856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87916240..88137540hg38UCSC Ensembl
chr9:90531155..90752455hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38221301
hg19221301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019387
Supporting Variants
Samples
Known GenesCDK20, SPATA31C1, SPATA31C2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588813
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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