A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3561119



Internal ID18512714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36060260..36124040hg38UCSC Ensembl
Innerchr17:34387619..34451426hg19UCSC Ensembl
Innerchr17:31411732..31475539hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3863781
hg1963808
hg1863808
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065440
Supporting Variants
Samples
Known GenesCCL18, CCL3, CCL4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3561119
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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