A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223822



Internal ID22367477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11954073..11954144hg38UCSC Ensembl
chr17:11857390..11857461hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14386848, nssv14388645
SamplesHG00731, HG00733
Known GenesDNAH9
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223822
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer