A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173393



Internal ID20740433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107221865..107222484hg38UCSC Ensembl
chr9:109984146..109984765hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444114
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173393
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00041


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