A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843825



Internal ID22618760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93419380..93421779hg38UCSC Ensembl
chr5:92755086..92757485hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499571
Samples
Known GenesNR2F1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843825
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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