A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642325



Internal ID21590630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149777791..149777791hg38UCSC Ensembl
chr5:149157354..149157354hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128237
SamplesHG03065
Known GenesPPARGC1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642325
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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