A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481020



Internal ID22538924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11593880..11595960hg38UCSC Ensembl
chrUn_gl000231:7891..9971hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382081
hg192081
Variant TypeOTHER copy number variation
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868102
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481020
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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