A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401614



Internal ID22459484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19487271..19487508hg38UCSC Ensembl
chr22:19474794..19475031hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5954728
Supporting Variants
Samples
Known GenesCDC45
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401614
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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