A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3556468



Internal ID22425293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24575756..24575756hg38UCSC Ensembl
chr16:24587077..24587077hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14419327
SamplesHG00514
Known Genes
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)nsv3556468
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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