A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032175



Internal ID18774709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160266174..162269517hg38UCSC Ensembl
Innerchr4:161187326..163190669hg19UCSC Ensembl
Innerchr4:161406776..163410119hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg382003344
hg192003344
hg182003344
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744445
Samples
Known GenesFSTL5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032175
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