A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366166



Internal ID22591835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179095258..179097563hg38UCSC Ensembl
chr1:179064393..179066698hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg382306
hg192306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876523
Supporting Variants
Samples
Known GenesTOR3A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366166
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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