A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5539531



Internal ID314467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122177656..122177656hg38UCSC Ensembl
chr10:123937171..123937171hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040391
Samples
Known GenesTACC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5539531
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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