A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070036



Internal ID18970776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57324425..57324926hg38UCSC Ensembl
chr11:57091899..57092400hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771702
SamplesKWP1
Known GenesTNKS1BP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070036
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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