A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554018



Internal ID16341427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37747707..37815386hg38UCSC Ensembl
Innerchr11:37769257..37836936hg19UCSC Ensembl
Innerchr11:37725833..37793512hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3867680
hg1967680
hg1867680
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1745n54
Supporting Variantsnssv771076, nssv771077
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554018
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer