A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566064



Internal ID16006787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104690606..104714228hg38UCSC Ensembl
Innerchr14:105156943..105180565hg19UCSC Ensembl
Innerchr14:104227988..104251610hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3823623
hg1923623
hg1823623
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834445
Samples
Known GenesINF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566064
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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