A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376420



Internal ID22602089
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 StatusS
Merged Variantsnsv5944837
Supporting Variants
Samples
Known GenesGFOD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376420
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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