A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5546972



Internal ID320868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103253069..103253119hg38UCSC Ensembl
chr10:105012826..105012876hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040006
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5546972
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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