A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225005



Internal ID22368270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100376101..100376167hg38UCSC Ensembl
chr10:102135858..102135924hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1031n152
Supporting Variantsnssv14384759
SamplesNA19240
Known GenesLINC00263
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225005
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer