A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206692



Internal ID22355200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63783072..63783835hg38UCSC Ensembl
chr10:65542832..65543595hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38764
hg19764
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv961n152
Supporting Variantsnssv14414210
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206692
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