A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3773026



Internal ID18959611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23119299..23219597hg38UCSC Ensembl
chr8:22976812..23077110hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38100299
hg19100299
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1068323
Supporting Variants
SamplesKWP1
Known GenesTNFRSF10A, TNFRSF10D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3773026
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