A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149591



Internal ID15508451
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 StatusS
Merged Variantsnsv569314
Supporting Variants
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)nssv1149591
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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