A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563807



Internal ID16351216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19889220..19932841hg38UCSC Ensembl
Innerchr14:20357379..20401000hg19UCSC Ensembl
Innerchr14:19427219..19470840hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3843622
hg1943622
hg1843622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3529n54
Supporting Variantsnssv821702, nssv821701
Samples
Known GenesOR4K5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563807
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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