A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3233634



Internal ID22372809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:2404215..2412365hg38UCSC Ensembl
Outerchr12:2513381..2521531hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg381168
hg191168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14256283
SamplesNA19239
Known GenesCACNA1C
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3233634
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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