A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766884



Internal ID18964531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125183212..125183546hg38UCSC Ensembl
chr11:125053108..125053442hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070993
Supporting Variants
SamplesKWP1
Known GenesPKNOX2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766884
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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