A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207196



Internal ID22355626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:30946727..30961102hg38UCSC Ensembl
Outerchr3:30988219..31002594hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg3814376
hg1914376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14270386
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207196
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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