A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184338



Internal ID20751378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98093536..98109539hg38UCSC Ensembl
chr9:100855818..100871821hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3816004
hg1916004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440548
Supporting Variants
Samples
Known GenesTRIM14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184338
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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