A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070965



Internal ID19325350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64252327..64253128hg38UCSC Ensembl
chr11:64019799..64020600hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764133
SamplesKWP1
Known GenesPLCB3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070965
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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