A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574757



Internal ID16015480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36076917..36109139hg38UCSC Ensembl
Innerchr17:34404277..34436532hg19UCSC Ensembl
Innerchr17:31428390..31460645hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3832223
hg1932256
hg1832256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5534n54
Supporting Variantsnssv869856
Samples
Known GenesCCL3, CCL4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574757
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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