A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491167



Internal ID268411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33377273..34316186hg38UCSC Ensembl
chr10:33666201..34605114hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38938914
hg19938914
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17033011
Samples
Known GenesLINC00838, PARD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491167
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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