A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224947



Internal ID22368229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76189283..76189359hg38UCSC Ensembl
chr15:76481624..76481700hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14385346
SamplesNA19239
Known GenesC15orf27
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224947
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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