A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070056



Internal ID19317888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78677054..78683555hg38UCSC Ensembl
chr11:78388099..78394600hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg386502
hg196502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772697
SamplesKWP1
Known GenesTENM4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070056
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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