A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943105



Internal ID22718549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77316703..77316761hg38UCSC Ensembl
chr13:77890838..77890896hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382554
Samples
Known GenesMYCBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943105
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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