A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645446



Internal ID21837493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17038072..17040380hg38UCSC Ensembl
chr22:17518962..17521270hg19UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg382309
hg192309
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056116
Supporting Variants
Samples
Known GenesCECR7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645446
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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