A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766564



Internal ID19305559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46122148..46123349hg38UCSC Ensembl
chr11:46143699..46144900hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070955
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766564
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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