A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401837



Internal ID22459707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:23300551..23300601hg38UCSC Ensembl
chr22:23642738..23642788hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5965072
Supporting Variants
Samples
Known GenesBCR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401837
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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