A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565080



Internal ID16352489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73063317..73079868hg38UCSC Ensembl
Innerchr14:73530025..73546576hg19UCSC Ensembl
Innerchr14:72599778..72616329hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3816552
hg1916552
hg1816552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3754n54
Supporting Variantsnssv829180
Samples
Known GenesRBM25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565080
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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