A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5505924



Internal ID282684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113679225..113732415hg38UCSC Ensembl
chr10:115438984..115492174hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3853191
hg1953191
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039161
Samples
Known GenesCASP7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5505924
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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