A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831932



Internal ID22606867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168634546..168636245hg38UCSC Ensembl
chr2:169491056..169492755hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1244n209
Supporting Variantsnssv17480657, nssv17488339
Samples
Known GenesCERS6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831932
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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