A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011581



Internal ID19100798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89902705..90095596hg38UCSC Ensembl
Innerchr3:89951855..90144746hg19UCSC Ensembl
Innerchr3:90034545..90227436hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38192892
hg19192892
hg18192892
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4811n100
Supporting Variantsnssv3603280
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)nsv1011581
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