A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17575760



Internal ID21767803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149777829..149777956hg38UCSC Ensembl
chr5:149157392..149157519hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6018380
Supporting Variants
Samples
Known GenesPPARGC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17575760
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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