A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460143



Internal ID22518029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18206398..18211061hg38UCSC Ensembl
chrUn_gl000212:35150..39813hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg384664
hg194664
Variant TypeOTHER copy number variation
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867179
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460143
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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