A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411772



Internal ID21069325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149805374..149811914hg38UCSC Ensembl
chr5:149184937..149191477hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg386541
hg196541
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213279
Samples
Known GenesPPARGC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411772
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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