A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126294



Internal ID18918305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:57597027..57598327hg38UCSC Ensembl
Outerchr11:57364500..57365800hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg381301
hg191301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984530
SamplesKWS1
Known GenesSERPING1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126294
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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