A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005479



Internal ID21914822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149809179..149809232hg38UCSC Ensembl
chr5:149188742..149188795hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559271
Samples
Known GenesPPARGC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005479
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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