A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3246851



Internal ID22376547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100420978..100426501hg38UCSC Ensembl
chr8:101433206..101438729hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg385524
hg195524
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14342122
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3246851
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