A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3188595



Internal ID22340334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94252275..94252331hg38UCSC Ensembl
chr3:93971119..93971175hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14463010
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)nsv3188595
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