A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3561933



Internal ID18513528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36112573..36215877hg38UCSC Ensembl
Innerchr17:34439966..34543331hg19UCSC Ensembl
Innerchr17:31464079..31567444hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38103305
hg19103366
hg18103366
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060707
Supporting Variants
Samples
Known GenesCCL3L1, CCL3L3, CCL4L1, CCL4L2, TBC1D3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3561933
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