A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564718



Internal ID16352127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44715831..44765957hg38UCSC Ensembl
Innerchr14:45185034..45235160hg19UCSC Ensembl
Innerchr14:44254784..44304910hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3850127
hg1950127
hg1850127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3693n54
Supporting Variantsnssv827660
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564718
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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