A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197869



Internal ID22347691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:76843853..76857155hg38UCSC Ensembl
Outerchr3:76893004..76906306hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3813303
hg1913303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14271006
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3197869
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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