A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176959



Internal ID20743999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1311699..1721505hg38UCSC Ensembl
chr9:1311699..1721505hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38409807
hg19409807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431563
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176959
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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