A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526936



Internal ID22396320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68418418..68418469hg38UCSC Ensembl
chr3:68467568..68467619hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14307405, nssv14307410, nssv14307406, nssv14307409, nssv14307408, nssv14307407
SamplesNA19239, HG00731, HG00732, HG00733, HG00513, HG00514
Known GenesFAM19A1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526936
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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