A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517358



Internal ID15444651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:95951695..95974988hg38UCSC Ensembl
Innerchr11:95684859..95708152hg19UCSC Ensembl
Innerchr11:95324507..95347800hg18UCSC Ensembl
Innerchr11:95324507..95347800hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3823294
hg1923294
hg1823294
hg1723294
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665836, nssv652235, nssv678467, nssv666295, nssv651810, nssv684094, nssv674846, nssv692867, nssv691219, nssv663721, nssv673501, nssv653238, nssv679892, nssv657655, nssv660988
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517358
Frequency
Sample Size2026
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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