A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010312



Internal ID21919655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146497556..146497634hg38UCSC Ensembl
chr5:145877119..145877197hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559248
Samples
Known GenesTCERG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010312
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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