A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833132



Internal ID22608067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24094695..24107490hg38UCSC Ensembl
chr2:24317565..24330360hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3812796
hg1912796
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483448
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833132
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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