A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871167



Internal ID22646104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49860902..49865153hg38UCSC Ensembl
chr22:50254550..50258801hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg384252
hg194252
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484272
Samples
Known GenesZBED4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871167
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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