A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569580



Internal ID16356989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57336901..57475784hg38UCSC Ensembl
Innerchr15:57629099..57767982hg19UCSC Ensembl
Innerchr15:55416391..55555274hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38138884
hg19138884
hg18138884
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4556n54
Supporting Variantsnssv843554
Samples
Known GenesCGNL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569580
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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