A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565593



Internal ID16353002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:93988023..93994487hg38UCSC Ensembl
Innerchr14:94454369..94460833hg19UCSC Ensembl
Innerchr14:93524122..93530586hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg386465
hg196465
hg186465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3860n54
Supporting Variantsnssv832537, nssv832535, nssv832536
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565593
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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