A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484766



Internal ID262173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27710843..27712318hg38UCSC Ensembl
chr10:27999772..28001247hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg381476
hg191476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17033336
Samples
Known GenesMKX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484766
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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