A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998855



Internal ID17291807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:20930940..20940639hg38UCSC Ensembl
Outerchr18:18510901..18520600hg19UCSC Ensembl
Cytoband18q11.1
Allele length
AssemblyAllele length
hg389700
hg199700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952690
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998855
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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