A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416076



Internal ID22473946
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 StatusS
Merged Variantsnsv5903006
Supporting Variants
Samples
Known GenesMIR5684
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416076
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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