A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223221



Internal ID22367058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:31965661..31978954hg38UCSC Ensembl
Outerchr10:32254589..32267882hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3813294
hg1913294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv860n152
Supporting Variantsnssv14276673
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223221
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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