A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535968



Internal ID311537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20350840..20350874hg38UCSC Ensembl
chr9:20350838..20350872hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17022410
Samples
Known GenesMLLT3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535968
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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