A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951847



Internal ID16954034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:110872443..110894242hg38UCSC Ensembl
Outerchr10:112632201..112654000hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3821800
hg1921800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998048
SamplesBILGI_BIOE
Known GenesPDCD4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951847
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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