A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574756



Internal ID16015479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36075679..36109139hg38UCSC Ensembl
Innerchr17:34403039..34436532hg19UCSC Ensembl
Innerchr17:31427152..31460645hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3833461
hg1933494
hg1833494
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5534n54
Supporting Variantsnssv1149361
Samples1780862402_A
Known GenesCCL3, CCL4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574756
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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