A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489018



Internal ID22546936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11596288..11604769hg38UCSC Ensembl
chrUn_gl000231:10299..18780hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg388482
hg198482
Variant TypeOTHER copy number variation
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870463
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489018
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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