A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033561



Internal ID19122782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2778668..2796335hg38UCSC Ensembl
Innerchr5:2778782..2796449hg19UCSC Ensembl
Innerchr5:2831782..2849449hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3817668
hg1917668
hg1817668
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638520
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)nsv1033561
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