A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3638529



Internal ID18936810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:4855545..4891513hg38UCSC Ensembl
Innerchr5:4855658..4891626hg19UCSC Ensembl
Innerchr5:4908658..4944626hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3835969
hg1935969
hg1835969
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028510
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3638529
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