A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564344



Internal ID16351753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35918522..35961257hg38UCSC Ensembl
Innerchr14:36387728..36430463hg19UCSC Ensembl
Innerchr14:35457479..35500214hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3842736
hg1942736
hg1842736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148948
SamplesHGDP00913
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564344
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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