A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5475498



Internal ID253133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20546225..20715429hg38UCSC Ensembl
chr10:20835154..21004358hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38169205
hg19169205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031716
Samples
Known GenesMIR4675
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5475498
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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