A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385755



Internal ID22443625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68971554..68971911hg38UCSC Ensembl
chr16:69005457..69005814hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5932700
Supporting Variants
Samples
Known GenesTANGO6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385755
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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