A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200637



Internal ID22350055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11282860..11285536hg38UCSC Ensembl
chr10:11324823..11327499hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382677
hg192677
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv800n152
Supporting Variantsnssv14412151, nssv14412152
SamplesNA19240
Known GenesCELF2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200637
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