A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3993391



Internal ID19229171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:15675175..15777710hg38UCSC Ensembl
Outerchr19:15785985..15888520hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38102536
hg19102536
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1141884
Supporting Variants
SamplesKWS2
Known GenesCYP4F12, CYP4F24P, OR10H2, OR10H3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3993391
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