A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16961872



Internal ID41884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15595205..15595311hg38UCSC Ensembl
chr5:15595314..15595420hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461894
Supporting Variants
Samples
Known GenesFBXL7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16961872
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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