A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517211



Internal ID15444504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35534425..35639794hg38UCSC Ensembl
Innerchr6:35502202..35607571hg19UCSC Ensembl
Innerchr6:35610180..35715549hg18UCSC Ensembl
Innerchr6:35610180..35715549hg17UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38105370
hg19105370
hg18105370
hg17105370
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv653101, nssv654020, nssv685313, nssv673440, nssv661085, nssv693945, nssv687535, nssv666166, nssv687600, nssv662028, nssv670258, nssv651751, nssv683963, nssv681980, nssv666568
Samples
Known GenesFKBP5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517211
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