A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5541286



Internal ID315908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68281489..68281528hg38UCSC Ensembl
chr15:68573827..68573866hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703897
Samples
Known GenesFEM1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5541286
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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