A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv827701



Internal ID16121657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:47120191..47184018hg38UCSC Ensembl
Innerchr14:47589394..47653221hg19UCSC Ensembl
Innerchr14:46659144..46722971hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3863828
hg1963828
hg1863828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564769
Supporting Variants
Samples
Known GenesMDGA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv827701
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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