A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997064



Internal ID18841876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:125426552..125426667hg38UCSC Ensembl
Outerchr11:125296448..125296563hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152458
Supporting Variants
SamplesKWB1
Known GenesPKNOX2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997064
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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