A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065113



Internal ID21974346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154373128..154373128hg38UCSC Ensembl
chr5:153752688..153752688hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571843
Samples
Known GenesGALNT10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065113
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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