A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759080



Internal ID20534940
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 StatusM
Merged Variants
Supporting Variantsnssv16284574
Samples
Known GenesPPARGC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759080
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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