A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703661



Internal ID15440313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:126372802..126376181hg38UCSC Ensembl
Innerchr11:126242697..126246076hg19UCSC Ensembl
Innerchr11:125747907..125751286hg18UCSC Ensembl
Innerchr11:125747907..125751286hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg383380
hg193380
hg183380
hg173380
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527257
Supporting Variants
Samples
Known GenesST3GAL4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703661
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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