A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020022



Internal ID19109241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3694651..3953484hg38UCSC Ensembl
Innerchr5:3694765..3953598hg19UCSC Ensembl
Innerchr5:3747765..4006598hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38258834
hg19258834
hg18258834
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638522
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)nsv1020022
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