A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15748531



Internal ID21387355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165761963..165762243hg38UCSC Ensembl
chr1:165731200..165731480hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432984
Supporting Variants
SamplesMDQ045
Known GenesTMCO1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15748531
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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