A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951858



Internal ID17300732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:118025690..118037989hg38UCSC Ensembl
Outerchr10:119785201..119797500hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3812300
hg1912300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998058
SamplesBILGI_BIOE
Known GenesRAB11FIP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951858
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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