A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862754



Internal ID22637689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20539890..20540889hg38UCSC Ensembl
chr9:20539889..20540888hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512193, nssv17512194
Samples
Known GenesMLLT3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862754
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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