A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490465



Internal ID267722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26171085..26176249hg38UCSC Ensembl
chr10:26460014..26465178hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg385165
hg195165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032286
Samples
Known GenesMYO3A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490465
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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