A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3247821



Internal ID22376806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:95575060..95608994hg38UCSC Ensembl
Outerchr12:95968836..96002770hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg382461
hg192461
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14255947, nssv14255946
SamplesNA19239, NA19240
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3247821
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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