A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831929



Internal ID22606864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16842528..16853893hg38UCSC Ensembl
chr2:17023795..17035160hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3811366
hg1911366
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488329
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831929
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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