A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035515



Internal ID19124734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61987149..62108238hg38UCSC Ensembl
Innerchr11:61754621..61875710hg19UCSC Ensembl
Innerchr11:61511197..61632286hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38121090
hg19121090
hg18121090
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1213n100
Supporting Variantsnssv3503862
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)nsv1035515
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