A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510237



Internal ID286862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124879502..124885600hg38UCSC Ensembl
chr10:126568071..126574169hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg386099
hg196099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038878
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510237
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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