A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3184295



Internal ID22338073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96132258..96132360hg38UCSC Ensembl
chr6:96580134..96580236hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14410718
SamplesNA19240
Known GenesFUT9
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3184295
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