A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110893



Internal ID19255335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:25799550..25814917hg38UCSC Ensembl
Outerchr12:25952484..25967851hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3815368
hg1915368
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961307
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110893
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