A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576309



Internal ID21768352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149777933..149777933hg38UCSC Ensembl
chr5:149157496..149157496hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6073310
Supporting Variants
Samples
Known GenesPPARGC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17576309
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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