A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234559



Internal ID20801599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15285772..15302761hg38UCSC Ensembl
chr9:15285770..15302759hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3816990
hg1916990
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426960
Supporting Variants
Samples
Known GenesTTC39B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234559
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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