A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574776



Internal ID16015499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36179341..36265379hg38UCSC Ensembl
Innerchr17:34506707..34610939hg19UCSC Ensembl
Innerchr17:31530820..31635052hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3886039
hg19104233
hg18104233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5540n54
Supporting Variantsnssv869900
Samples
Known GenesCCL3L1, CCL3L3, CCL4L1, CCL4L2, TBC1D3H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574776
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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