A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5480604



Internal ID258108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72475436..72496371hg38UCSC Ensembl
chr10:74235194..74256129hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3820936
hg1920936
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037532
Samples
Known GenesMICU1, MIR1256
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5480604
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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