A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094545



Internal ID22003778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52172767..52172767hg38UCSC Ensembl
chr13:52746902..52746902hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608857
Samples
Known GenesMRPS31P5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094545
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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