A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292086



Internal ID20501304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44825665..44825665hg38UCSC Ensembl
chr10:45321113..45321113hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756038
Supporting Variants
Samples
Known GenesTMEM72-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292086
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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