A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv827894



Internal ID16121850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:54232948..54246875hg38UCSC Ensembl
Innerchr14:54699666..54713593hg19UCSC Ensembl
Innerchr14:53769416..53783343hg18UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg3813928
hg1913928
hg1813928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564850
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)nssv827894
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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