A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513826



Internal ID290339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124873205..124873587hg38UCSC Ensembl
chr10:126561774..126562156hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038876
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513826
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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