A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513720



Internal ID290236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28411676..28415929hg38UCSC Ensembl
chr13:28985813..28990066hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg384254
hg194254
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686479
Samples
Known GenesFLT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513720
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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