A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569314



Internal ID16010037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:45128520..45158125hg38UCSC Ensembl
Innerchr15:45420718..45450323hg19UCSC Ensembl
Innerchr15:43208010..43237615hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3829606
hg1929606
hg1829606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842458, nssv1149591
Samples1780862456_A
Known GenesDUOX1, DUOXA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569314
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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