A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843363



Internal ID22618298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57473036..57477608hg38UCSC Ensembl
chr5:56768863..56773435hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg384573
hg194573
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497423
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843363
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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