A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489200



Internal ID266488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24758742..24772451hg38UCSC Ensembl
chr10:25047671..25061380hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3813710
hg1913710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17683737
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489200
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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