A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17590685



Internal ID21782728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15613392..16055548hg38UCSC Ensembl
chr9:15613390..16055546hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38442157
hg19442157
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014523
Supporting Variants
Samples
Known GenesCCDC171
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17590685
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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