A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1116504



Internal ID19266819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:50278804..50301955hg38UCSC Ensembl
Outerchr13:50852940..50876091hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3823152
hg1923152
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv970n106
Supporting Variantsnssv3978689
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1116504
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