A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839538



Internal ID22614473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:31291679..31297637hg38UCSC Ensembl
chr4:31293301..31299259hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg385959
hg195959
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493476
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839538
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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