A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746687



Internal ID19044968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:179629474..179677587hg38UCSC Ensembl
Innerchr5:179056475..179104588hg19UCSC Ensembl
Innerchr5:178989081..179037194hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3848114
hg1948114
hg1848114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021275
Supporting Variants
Samples
Known GenesC5orf60
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3746687
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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