A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831906



Internal ID22606841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16122949..16128517hg38UCSC Ensembl
chr2:16263071..16268639hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg385569
hg195569
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480604
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831906
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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