A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565858



Internal ID16353267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100722868..100766909hg38UCSC Ensembl
Innerchr14:101189205..101233246hg19UCSC Ensembl
Innerchr14:100258958..100302999hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3844042
hg1944042
hg1844042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv833677
Samples
Known GenesDLK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565858
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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