A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5425066



Internal ID204039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:166624516..166631553hg38UCSC Ensembl
chr1:166593753..166600790hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg387038
hg197038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16891564
Samples
Known GenesFMO9P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5425066
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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