A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565056



Internal ID16352465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73061922..73079971hg38UCSC Ensembl
Innerchr14:73528630..73546679hg19UCSC Ensembl
Innerchr14:72598383..72616432hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3818050
hg1918050
hg1818050
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3754n54
Supporting Variantsnssv829110
Samples
Known GenesRBM25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565056
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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