A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568771



Internal ID16009494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31064935..31092594hg38UCSC Ensembl
Innerchr15:31357138..31384797hg19UCSC Ensembl
Innerchr15:29144430..29172089hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3827660
hg1927660
hg1827660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4428n54
Supporting Variantsnssv1149554
Samples1780854419_A
Known GenesMIR211, TRPM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568771
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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