A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997791



Internal ID17290743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:89918184..89924483hg38UCSC Ensembl
Outerchr5:89214001..89220300hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg386300
hg196300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950102
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997791
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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