A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3552692



Internal ID22421584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90884772..90884772hg38UCSC Ensembl
chr9:93647054..93647054hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14429457
SamplesHG00514
Known GenesSYK
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)nsv3552692
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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