A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2469n106



Internal ID20161826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45618141..47590995hg38UCSC Ensembl
chr22:46014021..47986744hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg381972855
hg191972724
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1120059, nsv1116471
SamplesKWS2, KWS1
Known GenesATXN10, C22orf26, CDPF1, CELSR1, CERK, GRAMD4, GTSE1, GTSE1-AS1, LINC00899, LOC150381, LOC730668, MIR3619, MIR4762, MIR4763, MIRLET7A3, MIRLET7B, MIRLET7BHG, PKDREJ, PPARA, TBC1D22A, TRMU, TTC38, WNT7B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2469n106
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