A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566204



Internal ID16006927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105376842..105479048hg38UCSC Ensembl
Innerchr14:105843179..105945385hg19UCSC Ensembl
Innerchr14:104914224..105016430hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38102207
hg19102207
hg18102207
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834804
Samples
Known GenesCRIP2, MTA1, PACS2, TEX22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566204
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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