A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141746



Internal ID340943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5368000..5378000hg38UCSC Ensembl
chr10:5409963..5419963hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3810001
hg1910001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030508
Samples
Known GenesUCN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141746
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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