A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566215



Internal ID16006938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105469042..105475136hg38UCSC Ensembl
Innerchr14:105935379..105941473hg19UCSC Ensembl
Innerchr14:105006424..105012518hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg386095
hg196095
hg186095
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3989n54
Supporting Variantsnssv834815
Samples
Known GenesCRIP2, MTA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566215
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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