A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3547795



Internal ID22416760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26278968..26278968hg38UCSC Ensembl
chr22:26674934..26674934hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14449208
SamplesHG00733
Known GenesSEZ6L
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)nsv3547795
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer