A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951254



Internal ID16953441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:22325772..22375371hg38UCSC Ensembl
Outerchr10:22614701..22664300hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3849600
hg1949600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997090
SamplesBILGI_BIOE
Known GenesBMI1, COMMD3-BMI1, SPAG6
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951254
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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