A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17545279



Internal ID21869634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:23844786..23844786hg38UCSC Ensembl
chr4:23846409..23846409hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6073406
Supporting Variants
Samples
Known GenesPPARGC1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17545279
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer