A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221574



Internal ID20788614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13944608..14163618hg38UCSC Ensembl
chr9:13944607..14163617hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38219011
hg19219011
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418029
Supporting Variants
Samples
Known GenesLINC00583, NFIB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221574
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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