A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3187499



Internal ID22339760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86958098..86958565hg38UCSC Ensembl
chr4:87879250..87879717hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg38468
hg19468
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14424907
SamplesHG00514
Known GenesAFF1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3187499
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer