A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3547386



Internal ID22416358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92428653..92428653hg38UCSC Ensembl
chr12:92822429..92822429hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14443622
SamplesHG00733
Known GenesCLLU1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3547386
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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