A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569972



Internal ID16357381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74352604..74364212hg38UCSC Ensembl
Innerchr15:74644945..74656553hg19UCSC Ensembl
Innerchr15:72431998..72443606hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3811609
hg1911609
hg1811609
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv845260
Samples
Known GenesCYP11A1, LOC729739
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569972
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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