A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3524824



Internal ID22394260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63270863..63270973hg38UCSC Ensembl
chr3:63256539..63256649hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14306658, nssv14306655, nssv14306654, nssv14306657, nssv14306656
SamplesNA19238, NA19239, HG00731, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3524824
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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