A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211999



Internal ID22359379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:35811115..35837161hg38UCSC Ensembl
Outerchr4:35812737..35838783hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3810639
hg1910639
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14274262
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211999
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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