A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481105



Internal ID258600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74099318..74099897hg38UCSC Ensembl
chr10:75859076..75859655hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38580
hg19580
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037002
Samples
Known GenesVCL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481105
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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