A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951115



Internal ID16953302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:25198385..25208784hg38UCSC Ensembl
Outerchr8:25055901..25066300hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3810400
hg1910400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998709
SamplesBILGI_BIOE
Known GenesDOCK5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951115
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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