A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069065



Internal ID18974307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87863542..87864043hg38UCSC Ensembl
chr10:89623299..89623800hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772328
SamplesKWP1
Known GenesPTEN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069065
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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