A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136123



Internal ID18928960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:12674353..12675053hg38UCSC Ensembl
Outerchr11:12695900..12696600hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3989729
SamplesKWS2
Known GenesTEAD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136123
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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