A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223869



Internal ID20790909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:9358815..9416854hg38UCSC Ensembl
chr9:9358815..9416854hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3858040
hg1958040
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425564
Supporting Variants
Samples
Known GenesPTPRD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223869
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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