A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479668



Internal ID257184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49157585..49171501hg38UCSC Ensembl
chr10:50365630..50379546hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3813917
hg1913917
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036041
Samples
Known GenesC10orf128
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479668
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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