A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565563



Internal ID16352972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:93115246..93116087hg38UCSC Ensembl
Innerchr14:93581591..93582432hg19UCSC Ensembl
Innerchr14:92651344..92652185hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38842
hg19842
hg18842
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3847n54
Supporting Variantsnssv832404, nssv832405, nssv832406
Samples
Known GenesITPK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565563
Frequency
Sample Size17421
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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