A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138082



Internal ID18922459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:122926204..122926283hg38UCSC Ensembl
Outerchr11:122796912..122796991hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3968735, nssv3982912
SamplesKWS2, KWS1
Known GenesC11orf63
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138082
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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