A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3212335



Internal ID22359620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49742433..49742501hg38UCSC Ensembl
chr10:50950479..50950547hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv928n152
Supporting Variantsnssv14344572
SamplesHG00733
Known GenesOGDHL
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3212335
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