A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191796



Internal ID22342455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48702488..48702773hg38UCSC Ensembl
chr4:48704505..48704790hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14313950
SamplesHG00733
Known GenesFRYL
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3191796
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