A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1068716



Internal ID19320386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:104960574..105038071hg38UCSC Ensembl
chr8:105972802..106050299hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3877498
hg1977498
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771316
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1068716
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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