A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830922



Internal ID22605857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:12189824..12194236hg38UCSC Ensembl
chr2:12329950..12334362hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg384413
hg194413
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485836
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830922
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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