A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564833



Internal ID16352242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48954196..49011216hg38UCSC Ensembl
Innerchr14:49423399..49480419hg19UCSC Ensembl
Innerchr14:48493149..48550169hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3857021
hg1957021
hg1857021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv827865
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564833
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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