A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012554



Internal ID19101771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:65722728..65764255hg38UCSC Ensembl
Innerchr4:66588446..66629973hg19UCSC Ensembl
Innerchr4:66271041..66312568hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3841528
hg1941528
hg1841528
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5238n100
Supporting Variantsnssv3740177
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)nsv1012554
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