A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3890n106



Internal ID22797718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:117861489..117863419hg38UCSC Ensembl
chr8:118873728..118875658hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg381931
hg191931
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1140389, nsv1110842
SamplesKWS2, KWS1
Known GenesEXT1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3890n106
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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