A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569986



Internal ID16010709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74427190..74430583hg38UCSC Ensembl
Innerchr15:74719531..74722924hg19UCSC Ensembl
Innerchr15:72506584..72509977hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg383394
hg193394
hg183394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4626n54
Supporting Variantsnssv845280
Samples
Known GenesSEMA7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569986
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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