A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646336



Internal ID21838383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17049349..17050993hg38UCSC Ensembl
chr22:17530239..17531883hg19UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg381645
hg191645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6055369
Supporting Variants
Samples
Known GenesCECR7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646336
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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