A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3187027



Internal ID22339511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:5967137..5967945hg38UCSC Ensembl
chr4:5968864..5969672hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38809
hg19809
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14450655
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3187027
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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