A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202416



Internal ID22351585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:53173414..53173487hg38UCSC Ensembl
chr1:53639086..53639159hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv218n152
Supporting Variantsnssv14363735
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202416
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