A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574795



Internal ID16015518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36202819..36212480hg38UCSC Ensembl
Innerchr17:34530219..34539882hg19UCSC Ensembl
Innerchr17:31554332..31563995hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg389662
hg199664
hg189664
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5545n54
Supporting Variantsnssv869964
Samples
Known GenesCCL4L1, CCL4L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574795
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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