A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565576



Internal ID16352985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:93872387..93889459hg38UCSC Ensembl
Innerchr14:94338733..94355805hg19UCSC Ensembl
Innerchr14:93408486..93425558hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3817073
hg1917073
hg1817073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149543
SamplesHGDP00857
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565576
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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