A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838348



Internal ID22613283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150337489..150339917hg38UCSC Ensembl
chr4:151258641..151261069hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382429
hg192429
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490303
Samples
Known GenesLRBA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838348
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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