A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1068293



Internal ID18971730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23189170..23194971hg38UCSC Ensembl
chr10:23478099..23483900hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg385802
hg195802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768557
SamplesKWP1
Known GenesPTF1A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1068293
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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