A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662382



Internal ID15399034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:36146064..36245332hg38UCSC Ensembl
Innerchr21:37518362..37617630hg19UCSC Ensembl
Innerchr21:36440232..36539500hg18UCSC Ensembl
Innerchr21:36440232..36539500hg17UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3899269
hg1999269
hg1899269
hg1799269
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516175
Supporting Variants
Samples
Known GenesCBR3, CBR3-AS1, DOPEY2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662382
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