A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211752



Internal ID22359213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:37184805..37350760hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38165956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1797n152
Supporting Variantsnssv14422321
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211752
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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