A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284574



Internal ID20493792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149777951..149777951hg38UCSC Ensembl
chr5:149157514..149157514hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759080
Supporting Variants
Samples
Known GenesPPARGC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284574
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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