A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133003



Internal ID18932181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:117134547..117210019hg38UCSC Ensembl
Outerchr11:117005263..117080735hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3875473
hg1975473
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv730n106
Supporting Variantsnssv3987800
SamplesKWS1
Known GenesLOC100652768, PAFAH1B2, PCSK7, SIDT2, TAGLN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133003
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