A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569686



Internal ID16357095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62414468..62415506hg38UCSC Ensembl
Innerchr15:62706667..62707705hg19UCSC Ensembl
Innerchr15:60493959..60494997hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381039
hg191039
hg181039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4568n54
Supporting Variantsnssv843935, nssv843932, nssv843933, nssv843934, nssv843936
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569686
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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