A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229457



Internal ID22371307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:29451612..29466623hg38UCSC Ensembl
Outerchr17:27778630..27793641hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3815012
hg1915012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14260941
SamplesNA19238
Known GenesTAOK1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229457
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