A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213563



Internal ID22360471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:29002236..29020001hg38UCSC Ensembl
Outerchr12:29155169..29172934hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3817766
hg1917766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14255553
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213563
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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