A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566351



Internal ID16353760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105671130..106649040hg38UCSC Ensembl
Innerchr14:106137467..107105043hg19UCSC Ensembl
Innerchr14:105208512..106176088hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38977911
hg19967577
hg18967577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148645
SamplesHGDP01103
Known GenesADAM6, ELK2AP, KIAA0125, LINC00221, LINC00226
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566351
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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