A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942978



Internal ID22718422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19977158..19981219hg38UCSC Ensembl
chr16:19988480..19992541hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg384062
hg194062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389137
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942978
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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