A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5480206



Internal ID257716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30807032..30826374hg38UCSC Ensembl
chr10:31095961..31115303hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3819343
hg1919343
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030469
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5480206
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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