A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564411



Internal ID16351820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38489763..38555853hg38UCSC Ensembl
Innerchr14:38958967..39025057hg19UCSC Ensembl
Innerchr14:38028718..38094808hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3866091
hg1966091
hg1866091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3648n54
Supporting Variantsnssv826028
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564411
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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