A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388909



Internal ID22446779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54665242..54667904hg38UCSC Ensembl
chr16:54699154..54701816hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg382663
hg192663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927833
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388909
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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