A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206559



Internal ID22355078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:34772964..34873863hg38UCSC Ensembl
Outerchr4:34774586..34875485hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38100900
hg19100900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14272796, nssv14272795
SamplesHG00731, HG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206559
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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