A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564410



Internal ID16351819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38475617..38569077hg38UCSC Ensembl
Innerchr14:38944821..39038281hg19UCSC Ensembl
Innerchr14:38014572..38108032hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3893461
hg1993461
hg1893461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3648n54
Supporting Variantsnssv826027
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564410
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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