A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17482212



Internal ID22540117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:24766507..24769372hg38UCSC Ensembl
chr22:25162474..25165339hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg382866
hg192866
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5883405
Supporting Variants
Samples
Known GenesPIWIL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17482212
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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