A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907883



Internal ID22683093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20497794..20566590hg38UCSC Ensembl
chr9:20497792..20566589hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3868797
hg1968798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431270
Samples
Known GenesMIR4474, MLLT3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907883
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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