A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883405



Internal ID22658384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:24766507..24769372hg38UCSC Ensembl
chr22:25162474..25165339hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg382866
hg192866
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482212
Samples
Known GenesPIWIL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883405
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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