A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076368



Internal ID19318070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127260535..127262136hg38UCSC Ensembl
chr10:129058799..129060400hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg381602
hg191602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768045
SamplesKWP1
Known GenesDOCK1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076368
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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