A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217345



Internal ID22363040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98446132..98446183hg38UCSC Ensembl
chr10:100205889..100205940hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352874
SamplesNA19238
Known GenesHPS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217345
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