A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466661



Internal ID244493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113487916..113491275hg38UCSC Ensembl
chr5:112823613..112826972hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg383360
hg193360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16973251
Samples
Known GenesMCC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466661
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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