A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838977



Internal ID22613912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3057761..3061676hg38UCSC Ensembl
chr4:3059488..3063403hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg383916
hg193916
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493458
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838977
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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