A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569531



Internal ID16356940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55363385..55364362hg38UCSC Ensembl
Innerchr15:55655583..55656560hg19UCSC Ensembl
Innerchr15:53442875..53443852hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38978
hg19978
hg18978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4546n54
Supporting Variantsnssv843374, nssv843375, nssv843376, nssv843377
Samples
Known GenesCCPG1, DYX1C1-CCPG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569531
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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