A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222097



Internal ID22366281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:37500875..37513891hg38UCSC Ensembl
Outerchr6:37468651..37481667hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38921
hg19921
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7859n152
Supporting Variantsnssv14276500, nssv14276501, nssv14276502
SamplesHG00512, NA19238, NA19239
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222097
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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