A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197506



Internal ID22347379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:84211854..84212044hg38UCSC Ensembl
chr13:84785989..84786179hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14415904
SamplesHG00514
Known GenesLINC00333
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3197506
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