A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5401741



Internal ID181117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21741533..21741584hg38UCSC Ensembl
chr10:22030462..22030513hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17033681
Samples
Known GenesMLLT10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5401741
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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