A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3195920



Internal ID22346022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:141631807..141632071hg38UCSC Ensembl
chr5:141011374..141011638hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14325839, nssv14325838
SamplesNA19238, HG00731
Known GenesHDAC3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3195920
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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