A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040226



Internal ID19129445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3416258..3607794hg38UCSC Ensembl
Innerchr11:3437488..3629024hg19UCSC Ensembl
Innerchr11:3394064..3585600hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38191537
hg19191537
hg18191537
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1017n100
Supporting Variantsnssv3706397
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)nsv1040226
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