A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3551131



Internal ID22420048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32564681..32564681hg38UCSC Ensembl
chr13:33138818..33138818hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14378176
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3551131
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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