A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13703215



Internal ID21225028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165761974..165762253hg38UCSC Ensembl
chr1:165731211..165731490hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2800905
Supporting Variants
Samples
Known GenesTMCO1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13703215
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.953125


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