A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225777



Internal ID22368803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:47076830..47091439hg38UCSC Ensembl
Outerchr8:47988453..48003062hg19UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg3814610
hg1914610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14279059
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225777
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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