A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479226



Internal ID256756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17526216..17527442hg38UCSC Ensembl
chr10:17568215..17569441hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg381227
hg191227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030419
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479226
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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