A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569311



Internal ID16356720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:45028851..45031066hg38UCSC Ensembl
Innerchr15:45321049..45323264hg19UCSC Ensembl
Innerchr15:43108341..43110556hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg382216
hg192216
hg182216
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842455
Samples
Known GenesSORD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569311
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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