A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17428467



Internal ID22486337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15638692..15640784hg38UCSC Ensembl
chr4:15640315..15642407hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg382093
hg192093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5889272
Supporting Variants
Samples
Known GenesFBXL5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17428467
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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