A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569239



Internal ID16009962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42908911..43099877hg38UCSC Ensembl
Innerchr15:43201109..43392075hg19UCSC Ensembl
Innerchr15:40988401..41179367hg18UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38190967
hg19190967
hg18190967
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4500n54
Supporting Variantsnssv842228
Samples
Known GenesTTBK2, UBR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569239
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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