A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070063



Internal ID19317399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93057983..93067427hg38UCSC Ensembl
chr11:92791149..92800593hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg389445
hg199445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764762
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070063
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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