A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv825094



Internal ID16119050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28138868..28208067hg38UCSC Ensembl
Innerchr14:28608074..28677273hg19UCSC Ensembl
Innerchr14:27677825..27747024hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3869200
hg1969200
hg1869200
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564153
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv825094
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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