A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639929



Internal ID21831976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:22557973..22558046hg38UCSC Ensembl
chr22:22900392..22900465hg19UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6051545
Supporting Variants
Samples
Known GenesPRAME
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639929
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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