A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843831



Internal ID22618766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96657959..96661358hg38UCSC Ensembl
chr5:95993663..95997062hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500129
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843831
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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