A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586413



Internal ID21534966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58493539..58493600hg38UCSC Ensembl
chr15:58785738..58785799hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094792
SamplesNA24385
Known GenesLIPC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586413
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer