A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173891



Internal ID20740931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11733393..11939779hg38UCSC Ensembl
chr9:11733393..11939779hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38206387
hg19206387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429088
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173891
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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