A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3004393



Internal ID17297345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:76347405..76347880hg38UCSC Ensembl
Outerchr14:76813748..76814223hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv957515
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3004393
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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