A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17408516



Internal ID22466386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:23234669..23235624hg38UCSC Ensembl
chr22:23576856..23577811hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38956
hg19956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5958693
Supporting Variants
Samples
Known GenesBCR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17408516
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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