A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197819



Internal ID22347653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:162306135..162379466hg38UCSC Ensembl
Outerchr4:163227287..163300618hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3873332
hg1973332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14275059
SamplesHG00512
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3197819
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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