A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17425907



Internal ID22483777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15603540..15606516hg38UCSC Ensembl
chr5:15603649..15606625hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg382977
hg192977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5902729
Supporting Variants
Samples
Known GenesFBXL7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17425907
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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