A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226099



Internal ID22369023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154676083..154676156hg38UCSC Ensembl
chr7:154467793..154467866hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14338055
SamplesNA19239
Known GenesDPP6
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226099
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