A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843932



Internal ID22618867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:99497428..99503454hg38UCSC Ensembl
chr5:98833132..98839158hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg386027
hg196027
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1701n209
Supporting Variantsnssv17500200
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843932
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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