A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402898



Internal ID22460768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:24774526..24795719hg38UCSC Ensembl
chr22:25170493..25191686hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3821194
hg1921194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5948263
Supporting Variants
Samples
Known GenesPIWIL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402898
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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