A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838663



Internal ID22613598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:164596257..164626518hg38UCSC Ensembl
chr4:165517409..165547670hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3830262
hg1930262
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493585
Samples
Known GenesMIR5684
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838663
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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