A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205106



Internal ID22353856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:184936249..184989852hg38UCSC Ensembl
Outerchr3:184654037..184707640hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg3853604
hg1953604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14270894
SamplesHG00732
Known GenesVPS8
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205106
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