A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069455



Internal ID18974615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15229759..15229868hg38UCSC Ensembl
chr10:15271758..15271867hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764035
SamplesKWP1
Known GenesFAM171A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069455
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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