A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129859



Internal ID18935618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:125183189..125183479hg38UCSC Ensembl
Outerchr11:125053085..125053375hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv734n106
Supporting Variantsnssv3964986
SamplesKWS1
Known GenesPKNOX2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129859
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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