A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214209



Internal ID22360928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:168584..267248hg38UCSC Ensembl
Outerchr7:168584..307214hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3898665
hg19138631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14277390, nssv14277391
SamplesHG00731, HG00732
Known GenesFAM20C
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214209
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