A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3203664



Internal ID22352636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:82396444..82531363hg38UCSC Ensembl
Outerchr3:82445595..82580514hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38134920
hg19134920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14271494
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3203664
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