A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485809



Internal ID263190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79299936..79299991hg38UCSC Ensembl
chr10:81059693..81059748hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038614
Samples
Known GenesZMIZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485809
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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