A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020311



Internal ID19109530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5682419..5718336hg38UCSC Ensembl
Innerchr5:5682532..5718449hg19UCSC Ensembl
Innerchr5:5735532..5771449hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3835918
hg1935918
hg1835918
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5555n100
Supporting Variantsnssv3638591
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)nsv1020311
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