A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841348



Internal ID22616283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11836..15783hg38UCSC Ensembl
chr5:11836..15783hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg383948
hg193948
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493758, nssv17493757
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841348
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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