A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110854



Internal ID18916009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:389195..574446hg38UCSC Ensembl
Outerchr11:389195..574446hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38185252
hg19185252
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv564n106
Supporting Variantsnssv3961264
SamplesKWS1
Known GenesANO9, C11orf35, HRAS, LOC143666, LRRC56, MIR210, MIR210HG, PKP3, PTDSS2, RASSF7, RNH1, SIGIRR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110854
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