A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903006



Internal ID22678170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:164596730..164607252hg38UCSC Ensembl
chr4:165517882..165528404hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3810523
hg1910523
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416076
Samples
Known GenesMIR5684
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903006
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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