A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569579



Internal ID16356988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57330402..57483608hg38UCSC Ensembl
Innerchr15:57622600..57775806hg19UCSC Ensembl
Innerchr15:55409892..55563098hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38153207
hg19153207
hg18153207
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4556n54
Supporting Variantsnssv843553
Samples
Known GenesCGNL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569579
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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