A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206142



Internal ID22354729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:223881733..223882167hg38UCSC Ensembl
chr2:224746450..224746884hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14297455
SamplesHG00513
Known GenesWDFY1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206142
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