A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560351



Internal ID333361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123367364..123367415hg38UCSC Ensembl
chr10:125126880..125126931hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040436
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560351
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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