A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565369



Internal ID16352778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:83356382..83405209hg38UCSC Ensembl
Innerchr14:83822726..83871553hg19UCSC Ensembl
Innerchr14:82892479..82941306hg18UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3848828
hg1948828
hg1848828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv831385, nssv831384
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565369
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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