A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479666



Internal ID257182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69444071..69454677hg38UCSC Ensembl
chr10:71203827..71214433hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3810607
hg1910607
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035128
Samples
Known GenesTSPAN15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479666
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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