A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569796



Internal ID16010519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67030906..67073284hg38UCSC Ensembl
Innerchr15:67323244..67365622hg19UCSC Ensembl
Innerchr15:65110298..65152676hg18UCSC Ensembl
Cytoband15q22.33
Allele length
AssemblyAllele length
hg3842379
hg1942379
hg1842379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv844320
Samples
Known GenesSMAD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569796
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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