A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569528



Internal ID16356937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55362214..55364362hg38UCSC Ensembl
Innerchr15:55654412..55656560hg19UCSC Ensembl
Innerchr15:53441704..53443852hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg382149
hg192149
hg182149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4545n54
Supporting Variantsnssv843344
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)nsv569528
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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