A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3236316



Internal ID22373545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114010817..114014480hg38UCSC Ensembl
chr10:115770576..115774239hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg383664
hg193664
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14354583, nssv14354584
SamplesHG00512, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3236316
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