A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953003



Internal ID16955190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:22575463..22586762hg38UCSC Ensembl
Outerchr20:22556101..22567400hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3811300
hg1911300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999939
SamplesBILGI_BIOE
Known GenesFOXA2, LINC00261
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953003
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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