A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022406



Internal ID82618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20305336..20349488hg38UCSC Ensembl
chr9:20305334..20349486hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3844153
hg1944153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488606
Supporting Variants
Samples
Known GenesMLLT3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022406
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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