A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042152



Internal ID19131371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54762047..54852259hg38UCSC Ensembl
Innerchr11:51267021..51357233hg19UCSC Ensembl
Innerchr11:51123597..51213809hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3890213
hg1990213
hg1890213
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1156n100
Supporting Variantsnssv3517811, nssv3516705
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)nsv1042152
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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