A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887791



Internal ID22662787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:171988906..171995482hg38UCSC Ensembl
chr5:171415910..171422486hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg386577
hg196577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413970
Samples
Known GenesFBXW11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887791
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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