A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209642



Internal ID22357684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12172503..12172568hg38UCSC Ensembl
chr10:12214502..12214567hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14457876
SamplesHG00733
Known GenesNUDT5
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3209642
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