A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17128237



Internal ID21467421
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 StatusS
Merged Variantsnsv5642325
Supporting Variants
SamplesHG03065
Known GenesPPARGC1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17128237
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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