A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564767



Internal ID16352176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:47116304..47198772hg38UCSC Ensembl
Innerchr14:47585507..47667975hg19UCSC Ensembl
Innerchr14:46655257..46737725hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3882469
hg1982469
hg1882469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3703n54
Supporting Variantsnssv827700
Samples
Known GenesMDGA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564767
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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