A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142488



Internal ID341688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24000..70000hg38UCSC Ensembl
chr10:69936..115940hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3846001
hg1946005
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029817
Samples
Known GenesTUBB8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142488
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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