A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140359



Internal ID19275200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:56021556..56051932hg38UCSC Ensembl
Outerchr5:55317384..55347759hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3830377
hg1930376
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3979067
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140359
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