A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468733



Internal ID22526622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:69653879..69656779hg38UCSC Ensembl
chr13:70228011..70230911hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg382901
hg192901
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850317
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468733
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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