A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656682



Internal ID21604987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42152650..42152650hg38UCSC Ensembl
chr13:42726786..42726786hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092331
SamplesNA24385
Known GenesDGKH
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656682
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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