A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18175478



Internal ID20742518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18427799..18428543hg38UCSC Ensembl
chr9:18427797..18428541hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38745
hg19745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418312
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18175478
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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