A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564570



Internal ID16351979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42492102..42579845hg38UCSC Ensembl
Innerchr14:42961305..43049048hg19UCSC Ensembl
Innerchr14:42031055..42118798hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3887744
hg1987744
hg1887744
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv827228
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564570
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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