A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952980



Internal ID17301854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:4169354..4176353hg38UCSC Ensembl
Outerchr20:4150001..4157000hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999916
SamplesBILGI_BIOE
Known GenesSMOX
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952980
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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