A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509327



Internal ID285985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:107459297..107459426hg38UCSC Ensembl
chr10:109219055..109219184hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038157
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509327
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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