A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835911



Internal ID22610846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31524891..31530165hg38UCSC Ensembl
chr3:31566383..31571657hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg385275
hg195275
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490666
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835911
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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