A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225837



Internal ID22368846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:166263109..166292719hg38UCSC Ensembl
Outerchr6:166676597..166706207hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg386981
hg196981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14279035, nssv14279034, nssv14279036
SamplesHG00731, NA19240, HG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225837
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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