A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564623



Internal ID16352032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42863867..42885658hg38UCSC Ensembl
Innerchr14:43333070..43354861hg19UCSC Ensembl
Innerchr14:42402820..42424611hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3821792
hg1921792
hg1821792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv827508
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564623
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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