A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769927



Internal ID18968344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12922184..12922462hg38UCSC Ensembl
chr11:12943731..12944009hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077839
Supporting Variants
SamplesKWP1
Known GenesTEAD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769927
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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