A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3534655



Internal ID22403930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153222057..153222057hg38UCSC Ensembl
chr4:154143209..154143209hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14398501, nssv14424932, nssv14452469
SamplesNA19240, HG00733, HG00514
Known GenesTRIM2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3534655
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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