A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415562



Internal ID22473432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15605797..15612262hg38UCSC Ensembl
chr4:15607420..15613885hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg386466
hg196466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5887961
Supporting Variants
Samples
Known GenesFBXL5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415562
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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