A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569529



Internal ID16356938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55362214..55364417hg38UCSC Ensembl
Innerchr15:55654412..55656615hg19UCSC Ensembl
Innerchr15:53441704..53443907hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg382204
hg192204
hg182204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4545n54
Supporting Variantsnssv843362, nssv843354, nssv843353, nssv843350, nssv843346, nssv843369, nssv843358, nssv843361, nssv843360, nssv843371, nssv843347, nssv843367, nssv843345, nssv843363, nssv843349, nssv843366, nssv843352, nssv843351, nssv843355, nssv843356, nssv843359, nssv843348, nssv843364, nssv843372, nssv843368, nssv843365, nssv843370, nssv843357
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)nsv569529
Frequency
Sample Size17421
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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