A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089333



Internal ID21998566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44995413..44995413hg38UCSC Ensembl
chr13:45569548..45569548hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607403
Samples
Known GenesGPALPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089333
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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