A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565086



Internal ID16352495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73063508..73080036hg38UCSC Ensembl
Innerchr14:73530216..73546744hg19UCSC Ensembl
Innerchr14:72599969..72616497hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3816529
hg1916529
hg1816529
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3754n54
Supporting Variantsnssv829191, nssv829190, nssv829188, nssv829189
Samples
Known GenesRBM25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565086
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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