A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475680



Internal ID22533578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11238916..11241908hg38UCSC Ensembl
chr16:11332773..11335765hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg382993
hg192993
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877468
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475680
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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