A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143771



Internal ID342972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68844791..68847447hg38UCSC Ensembl
chr10:70604547..70607203hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382657
hg192657
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035633
Samples
Known GenesSTOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143771
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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