A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069618



Internal ID18970382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102110368..102112669hg38UCSC Ensembl
chr11:101981099..101983400hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg382302
hg192302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764337
SamplesKWP1
Known GenesYAP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069618
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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