A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5553828



Internal ID327036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27725080..27725116hg38UCSC Ensembl
chr13:28299217..28299253hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686439
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5553828
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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