A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838378



Internal ID22613313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158475933..158477980hg38UCSC Ensembl
chr4:159397085..159399132hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg382048
hg192048
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490699
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838378
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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