A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076381



Internal ID19325702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95542035..95546236hg38UCSC Ensembl
chr11:95275199..95279400hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg384202
hg194202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769910
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076381
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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