A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838372



Internal ID22613307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157700319..157720504hg38UCSC Ensembl
chr4:158621471..158641656hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3820186
hg1920186
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499740
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838372
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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