A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1068286



Internal ID18971124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17452700..17454501hg38UCSC Ensembl
chr10:17494699..17496500hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg381802
hg191802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766087
SamplesKWP1
Known GenesST8SIA6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1068286
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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