A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412766



Internal ID22470636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15644708..15655202hg38UCSC Ensembl
chr4:15646331..15656825hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3810495
hg1910495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901882
Supporting Variants
Samples
Known GenesFBXL5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412766
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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