A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574755



Internal ID16015478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36025629..36153146hg38UCSC Ensembl
Innerchr17:34352666..34480526hg19UCSC Ensembl
Innerchr17:31376779..31504639hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38127518
hg19127861
hg18127861
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv869855
Samples
Known GenesCCL18, CCL3, CCL4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574755
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer