A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150134



Internal ID18855614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:120516992..120517668hg38UCSC Ensembl
Outerchr11:120387701..120388377hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003435
SamplesKWB1
Known GenesGRIK4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150134
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