A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3184279



Internal ID22338063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:27731317..27731376hg38UCSC Ensembl
chr4:27732939..27732998hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14397875
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)nsv3184279
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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