A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146235



Internal ID18855706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:123128374..123128502hg38UCSC Ensembl
Outerchr11:122999082..122999210hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999438
SamplesKWB1
Known GenesCLMP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146235
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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