A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564472



Internal ID16351881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:41130185..41189664hg38UCSC Ensembl
Innerchr14:41599390..41658867hg19UCSC Ensembl
Innerchr14:40669140..40728617hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3859480
hg1959478
hg1859478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3659n54
Supporting Variantsnssv826666
Samples
Known GenesLOC644919
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564472
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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