A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1127199



Internal ID19281382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:65306431..65306504hg38UCSC Ensembl
Outerchr11:65073902..65073975hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985578
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1127199
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer