A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483116



Internal ID15235590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100674835..100852920hg38UCSC Ensembl
Innerchr14:101141172..101319257hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38178086
hg19178086
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2995917
Samples
Known GenesDLK1, MEG3, MIR2392, MIR770
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483116
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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