A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961037



Internal ID18866616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:106709911..106709971hg38UCSC Ensembl
Outerchr11:106580637..106580697hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125532
Supporting Variants
SamplesKWS1
Known GenesGUCY1A2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961037
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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