A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224740



Internal ID20791780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15288256..15372749hg38UCSC Ensembl
chr9:15288254..15372747hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3884494
hg1984494
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422088
Supporting Variants
Samples
Known GenesTTC39B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224740
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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