A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3211n106



Internal ID22797039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170170463..170171983hg38UCSC Ensembl
chr5:169597467..169598987hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg381521
hg191521
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1125287, nsv1125294, nsv1110839
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3211n106
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