A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415392



Internal ID21072945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148403843..148404406hg38UCSC Ensembl
chr5:147783406..147783969hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125937
Samples
Known GenesFBXO38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415392
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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