A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092344



Internal ID22001577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42152650..42152650hg38UCSC Ensembl
chr13:42726786..42726786hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599854
Samples
Known GenesDGKH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092344
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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