A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3203567



Internal ID22352551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8559423..8560126hg38UCSC Ensembl
chr3:8601109..8601812hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38704
hg19704
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14304571, nssv14304572
SamplesNA19239, NA19240
Known GenesLMCD1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3203567
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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