A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517555



Internal ID293975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48396874..48409000hg38UCSC Ensembl
chr15:48689071..48701197hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3812127
hg1912127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17699822
Samples
Known GenesFBN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517555
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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