A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17483627



Internal ID22541534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43109171..43119713hg38UCSC Ensembl
chr22:43505177..43515719hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3810543
hg1910543
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879737
Supporting Variants
Samples
Known GenesBIK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17483627
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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