A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550779



Internal ID15991502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46224041..46306785hg38UCSC Ensembl
Innerchr10:47595277..47678021hg19UCSC Ensembl
Innerchr10:47065283..47148027hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3882745
hg1982745
hg1882745
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1116n54
Supporting Variantsnssv747550
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550779
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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