A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195233



Internal ID20762273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79413201..79415400hg38UCSC Ensembl
chr9:82028116..82030315hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446500
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195233
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0009


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