A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564138



Internal ID16351547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27885392..27972675hg38UCSC Ensembl
Innerchr14:28354598..28441881hg19UCSC Ensembl
Innerchr14:27424438..27511721hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3887284
hg1987284
hg1887284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3596n54
Supporting Variantsnssv1149484
SamplesHGDP01053
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564138
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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