A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015505



Internal ID18758039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161989825..163516137hg38UCSC Ensembl
Innerchr4:162910977..164437289hg19UCSC Ensembl
Innerchr4:163130427..164656739hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg381526313
hg191526313
hg181526313
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3634150
Samples
Known GenesFSTL5, NAF1, NPY1R, NPY5R, TKTL2, TMA16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015505
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