A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5534618



Internal ID310394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112304742..112304787hg38UCSC Ensembl
chr10:114064500..114064545hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039709
Samples
Known GenesTECTB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5534618
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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