A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205284



Internal ID22354000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:106665940..106703561hg38UCSC Ensembl
Outerchr5:106001641..106039262hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3837622
hg1937622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14274696
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205284
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