A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944837



Internal ID22720308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67707197..67707506hg38UCSC Ensembl
chr16:67741100..67741409hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376420
Samples
Known GenesGFOD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944837
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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