A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054880



Internal ID19144099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97428102..97509648hg38UCSC Ensembl
Innerchr11:97299102..97380648hg19UCSC Ensembl
Innerchr11:96804312..96885858hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3881547
hg1981547
hg1881547
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1259n100
Supporting Variantsnssv3517889
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)nsv1054880
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